Introduction to Hereditary Hemochromatosis
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Hereditary Hemochromatosis sentence examples within nonalcoholic fatty liver
Recently, ferroptosis has been involved in the pathological process of nonviral liver diseases [including alcohol-related liver disease (ALD); nonalcoholic fatty liver disease (NAFLD); hereditary hemochromatosis (HH); drug-, ischemia/reperfusion- or immune-induced liver injury; liver fibrosis; and liver cancer].
Recently, ferroptosis has been involved in the pathological process of nonviral liver diseases [including alcohol-related liver disease (ALD); nonalcoholic fatty liver disease (NAFLD); hereditary hemochromatosis (HH); drug-, ischemia/reperfusion- or immune-induced liver injury; liver fibrosis; and liver cancer].
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Besides identified risk factors for HCC including chronic infection with hepatitis B and C virus (HBV and HCV), alcohol abuse, dietary aflatoxin exposure and hereditary hemochromatosis, nonalcoholic fatty liver disease (NAFLD) is as another important risk factor for HCC.
Besides identified risk factors for HCC including chronic infection with hepatitis B and C virus (HBV and HCV), alcohol abuse, dietary aflatoxin exposure and hereditary hemochromatosis, nonalcoholic fatty liver disease (NAFLD) is as another important risk factor for HCC.
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Hereditary Hemochromatosis sentence examples within autosomal recessive disorder
Background Hereditary hemochromatosis is an autosomal recessive disorder where the clinical phenotype of skin pigmentation and organ damage occurs only in homozygotes.
Background Hereditary hemochromatosis is an autosomal recessive disorder where the clinical phenotype of skin pigmentation and organ damage occurs only in homozygotes.
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Background and Aims: Hereditary hemochromatosis (HH) is an autosomal recessive disorder, characterized by increased intestinal absorption of iron.
Background and Aims: Hereditary hemochromatosis (HH) is an autosomal recessive disorder, characterized by increased intestinal absorption of iron.
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Hereditary Hemochromatosis sentence examples within systemic iron overload
Hereditary Hemochromatosis (HH) is a genetic condition associated with a systemic iron overload.
Hereditary Hemochromatosis (HH) is a genetic condition associated with a systemic iron overload.
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Hereditary hemochromatosis (HH) is a genetic condition associated with a systemic iron overload caused by a reduction in the concentration of the iron regulatory hormone hepcidin or the hepcidin-ferroportin complex activity.
Hereditary hemochromatosis (HH) is a genetic condition associated with a systemic iron overload caused by a reduction in the concentration of the iron regulatory hormone hepcidin or the hepcidin-ferroportin complex activity.
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Hereditary Hemochromatosis sentence examples within autosomal recessive genetic
Hereditary Hemochromatosis sentence examples within inherited iron overload
Hereditary Hemochromatosis sentence examples within 1 antitrypsin deficiency
Methods Data were abstracted from the National Inpatient Sample database between 2002 and 2014 using ICD9 codes for patients discharged with NACLD and NALC secondary to genetic diseases including alpha-1 antitrypsin deficiency (A1ATd), cystic fibrosis (CF), Wilson disease (WD), hereditary hemochromatosis (HHC), glycogen storage disease, and disorders of aromatic amino-acid metabolism (DAAAM).
Methods Data were abstracted from the National Inpatient Sample database between 2002 and 2014 using ICD9 codes for patients discharged with NACLD and NALC secondary to genetic diseases including alpha-1 antitrypsin deficiency (A1ATd), cystic fibrosis (CF), Wilson disease (WD), hereditary hemochromatosis (HHC), glycogen storage disease, and disorders of aromatic amino-acid metabolism (DAAAM).
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In April 2017, the FDA authorized 23andMe to market genetic health risk tests for 10 conditions (Parkinson disease, late-onset Alzheimer disease, celiac disease, 1-antitrypsin deficiency, early-onset primary dystonia, factor XI deficiency, Gaucher disease type 1, glucose-6-phosphate dehydrogenase deficiency, hereditary hemochromatosis, and hereditary thrombophilia) (3).
In April 2017, the FDA authorized 23andMe to market genetic health risk tests for 10 conditions (Parkinson disease, late-onset Alzheimer disease, celiac disease, 1-antitrypsin deficiency, early-onset primary dystonia, factor XI deficiency, Gaucher disease type 1, glucose-6-phosphate dehydrogenase deficiency, hereditary hemochromatosis, and hereditary thrombophilia) (3).
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Hereditary Hemochromatosis sentence examples within iron overload disorder
Genetic diseases that decrease hepcidin synthesis or disrupt hepcidin binding to ferroportin cause the iron overload disorder hereditary hemochromatosis.
Genetic diseases that decrease hepcidin synthesis or disrupt hepcidin binding to ferroportin cause the iron overload disorder hereditary hemochromatosis.
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The HFE gene encodes for a protein involved in iron metabolism, while genetic variants in HFE have been associated with hereditary hemochromatosis (HH), an iron overload disorder.
The HFE gene encodes for a protein involved in iron metabolism, while genetic variants in HFE have been associated with hereditary hemochromatosis (HH), an iron overload disorder.
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Hereditary Hemochromatosis sentence examples within fatty liver disease
This review discusses the association of iron with metabolic disorders such as hereditary hemochromatosis, non-alcoholic fatty liver disease, obesity, and type 2 diabetes, in the background of hepatocellular carcinoma.
This review discusses the association of iron with metabolic disorders such as hereditary hemochromatosis, non-alcoholic fatty liver disease, obesity, and type 2 diabetes, in the background of hepatocellular carcinoma.
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Hereditary Hemochromatosis sentence examples within Background Hereditary Hemochromatosis
Background Hereditary hemochromatosis is an autosomal recessive disorder where the clinical phenotype of skin pigmentation and organ damage occurs only in homozygotes.
Background Hereditary hemochromatosis is an autosomal recessive disorder where the clinical phenotype of skin pigmentation and organ damage occurs only in homozygotes.
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Background Hereditary hemochromatosis is a heterogenous group of inherited iron-overload conditions that is characterized by increased intestinal absorption and deposition in vital organs.
Background Hereditary hemochromatosis is a heterogenous group of inherited iron-overload conditions that is characterized by increased intestinal absorption and deposition in vital organs.
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Hereditary Hemochromatosis sentence examples within Disorder Hereditary Hemochromatosis
Genetic diseases that decrease hepcidin synthesis or disrupt hepcidin binding to ferroportin cause the iron overload disorder hereditary hemochromatosis.
Genetic diseases that decrease hepcidin synthesis or disrupt hepcidin binding to ferroportin cause the iron overload disorder hereditary hemochromatosis.
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In the genetic, iron-loading disorder hereditary hemochromatosis (HH), hepcidin production is low and Fpn1 protein expression is elevated.
In the genetic, iron-loading disorder hereditary hemochromatosis (HH), hepcidin production is low and Fpn1 protein expression is elevated.
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10.31557/APJCP.2021.22.9.2837
BACKGROUND
Hereditary hemochromatosis is a genetic disease defined by enhanced overloading of iron and associated with Chronic Hepatitis C (CHC).
BACKGROUND
Hereditary hemochromatosis is a genetic disease defined by enhanced overloading of iron and associated with Chronic Hepatitis C (CHC).
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10.1002/jcp.30383
Lastly, it elaborates on the involvement of MSCs in the pathology of clinical conditions of iron‐excess, namely, hereditary hemochromatosis, diabetes, β‐thalassaemia and myelodysplastic syndromes.
Lastly, it elaborates on the involvement of MSCs in the pathology of clinical conditions of iron‐excess, namely, hereditary hemochromatosis, diabetes, β‐thalassaemia and myelodysplastic syndromes.
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10.7759/cureus.18067
Hereditary hemochromatosis is not a common cause of AVN but should be considered prior to labeling such cases as idiopathic.
Hereditary hemochromatosis is not a common cause of AVN but should be considered prior to labeling such cases as idiopathic.
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10.37421/2165-7831.2021.11.257
Hereditary Hemochromatosis is diseases caused due to abnormality in genes.
Hereditary Hemochromatosis is diseases caused due to abnormality in genes.
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10.4103/JCMRP.JCMRP_98_19
The link between iron and diabetes was first recognized in pathologic conditions such as hereditary hemochromatosis and thalassemia.
The link between iron and diabetes was first recognized in pathologic conditions such as hereditary hemochromatosis and thalassemia.
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10.1097/MD.0000000000025258
Rationale: Hereditary hemochromatosis (HH) is a hereditary disorder of iron metabolism.
Rationale: Hereditary hemochromatosis (HH) is a hereditary disorder of iron metabolism.
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10.1016/j.endien.2021.08.006
This article reviews endocrine changes in the main four diseases at epidemiological level: sarcoidosis, Langerhans cell histiocytosis, hereditary hemochromatosis, and systemic amyloidosis.
This article reviews endocrine changes in the main four diseases at epidemiological level: sarcoidosis, Langerhans cell histiocytosis, hereditary hemochromatosis, and systemic amyloidosis.
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10.1039/d1fo00482d
This study proposed to investigate the effect of Ilex paraguariensis infusion on the absorption of non-heme iron in hereditary hemochromatosis (HH) patients with the HFE genotype.
This study proposed to investigate the effect of Ilex paraguariensis infusion on the absorption of non-heme iron in hereditary hemochromatosis (HH) patients with the HFE genotype.
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10.5935/1676-2444.20210017
Hereditary hemochromatosis (HH) is an autosomal recessive disease, most often associated with mutations in the HFE gene, which result in continuous absorption of iron, causing its overload.
Hereditary hemochromatosis (HH) is an autosomal recessive disease, most often associated with mutations in the HFE gene, which result in continuous absorption of iron, causing its overload.
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10.3390/diagnostics11071279
Hereditary hemochromatosis (HH) is a genetic disease leading to excessive iron absorption, its accumulation, and oxidative stress induction causing different organ damage, including the heart.
Hereditary hemochromatosis (HH) is a genetic disease leading to excessive iron absorption, its accumulation, and oxidative stress induction causing different organ damage, including the heart.
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10.1007/s00261-020-02912-w
Liver, spleen, and bone marrow R2* were higher in thalassemia than in hereditary hemochromatosis (all p < 0.
Liver, spleen, and bone marrow R2* were higher in thalassemia than in hereditary hemochromatosis (all p < 0.
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10.1053/j.seminhematol.2021.06.002
Recent studies have shown that not only iron itself, but also iron-regulatory proteins that are mutated in hereditary hemochromatosis can control bone mass.
Recent studies have shown that not only iron itself, but also iron-regulatory proteins that are mutated in hereditary hemochromatosis can control bone mass.
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10.36295/ASRO.2020.232364
Hereditary hemochromatosis (HH) resulting from HFE gene mutation is the most common form.
Hereditary hemochromatosis (HH) resulting from HFE gene mutation is the most common form.
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10.1002/ccr3.4907
The patient was ultimately diagnosed with both polycythemia vera and hereditary hemochromatosis.
The patient was ultimately diagnosed with both polycythemia vera and hereditary hemochromatosis.
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10.1177/1078155221994322
The patient presented by Triesel and colleagues had a history of hereditary hemochromatosis, a disorder of iron overload.
The patient presented by Triesel and colleagues had a history of hereditary hemochromatosis, a disorder of iron overload.
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10.1186/s13023-021-02036-4
Additional factors to be considered are the possible association with bone marrow, renal or hepatic diseases, other causes of iron overload (hereditary hemochromatosis, hemoglobinopathies, metabolic diseases), and the presence of extra-hematological signs/symptoms.
Additional factors to be considered are the possible association with bone marrow, renal or hepatic diseases, other causes of iron overload (hereditary hemochromatosis, hemoglobinopathies, metabolic diseases), and the presence of extra-hematological signs/symptoms.
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10.5455/mjhs.2021.03.012
In hereditary hemochromatosis type II hepcidin production is low due to gene mutation that leads to iron overload.
In hereditary hemochromatosis type II hepcidin production is low due to gene mutation that leads to iron overload.
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10.51161/REMS/613
Material e metodos: Foram utilizados a base de dados Pubmed e os descritores "hereditary hemochromatosis" e "diabetes mellitus", encontrando-se 35 artigos dos ultimos 10 anos.
Material e metodos: Foram utilizados a base de dados Pubmed e os descritores "hereditary hemochromatosis" e "diabetes mellitus", encontrando-se 35 artigos dos ultimos 10 anos.
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10.1038/s41392-021-00696-z
The phenotype is similar to that seen in mild forms of hereditary hemochromatosis caused by genetic regulatory lesions that impair iron-induced hepcidin synthesis.
The phenotype is similar to that seen in mild forms of hereditary hemochromatosis caused by genetic regulatory lesions that impair iron-induced hepcidin synthesis.
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10.5603/EP.a2021.0008
INTRODUCTION
Hereditary hemochromatosis (HH) is a disease characterized by the excessive absorption of iron and its deposition in various organs.
INTRODUCTION
Hereditary hemochromatosis (HH) is a disease characterized by the excessive absorption of iron and its deposition in various organs.
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10.1002/hep4.1780
Genetic hepcidin inactivation leads to hereditary hemochromatosis, a disease of iron overload.
Genetic hepcidin inactivation leads to hereditary hemochromatosis, a disease of iron overload.
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10.1152/ajpgi.00371.2020
Phlebotomies are performed in hereditary hemochromatosis (HH) to maintain normal iron concentrations.
Phlebotomies are performed in hereditary hemochromatosis (HH) to maintain normal iron concentrations.
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10.1016/j.tips.2021.05.001
We here summarize recent progress in the pathophysiology and pharmacology of iron-overload diseases, such as hereditary hemochromatosis, as well as iron-deficiency disorders, which are typically associated with anemia.
We here summarize recent progress in the pathophysiology and pharmacology of iron-overload diseases, such as hereditary hemochromatosis, as well as iron-deficiency disorders, which are typically associated with anemia.
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10.1002/cld.1051
These can be inherited (hereditary hemochromatosis [HH]) or secondary to a number of conditions, such as multiple blood transfusions, dyserythropoiesis, and chronic liver disease.
These can be inherited (hereditary hemochromatosis [HH]) or secondary to a number of conditions, such as multiple blood transfusions, dyserythropoiesis, and chronic liver disease.
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10.1002/jmri.27643
Hepatic iron overload is characteristic of hereditary hemochromatosis or secondary hemosiderosis.
Hepatic iron overload is characteristic of hereditary hemochromatosis or secondary hemosiderosis.
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10.1093/clinchem/hvab130
BACKGROUND
Hereditary hemochromatosis (HH) is a genetic disease, leading to iron accumulation and possible organ damage.
BACKGROUND
Hereditary hemochromatosis (HH) is a genetic disease, leading to iron accumulation and possible organ damage.
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10.3389/fneur.2021.609236
Iron overload cardiomyopathy is the leading cause of death in patients with iron overload secondary to chronic blood transfusion therapy; it is also described in hereditary hemochromatosis.
Iron overload cardiomyopathy is the leading cause of death in patients with iron overload secondary to chronic blood transfusion therapy; it is also described in hereditary hemochromatosis.
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10.1007/s12011-020-02508-x
Iron overload has been found very common in diseases such as hereditary hemochromatosis, thalassemia, and sickle cell disease and in healthy postmenopausal women.
Iron overload has been found very common in diseases such as hereditary hemochromatosis, thalassemia, and sickle cell disease and in healthy postmenopausal women.
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10.1016/j.clinre.2021.101658
INTRODUCTION AND OBJECTIVES
The goal of this study was to assess lifestyle habits and physician counseling of patients with hereditary hemochromatosis (HH), and determine the prevalence of direct-to-consumer (DTC) genetic testing.
INTRODUCTION AND OBJECTIVES
The goal of this study was to assess lifestyle habits and physician counseling of patients with hereditary hemochromatosis (HH), and determine the prevalence of direct-to-consumer (DTC) genetic testing.
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10.26402/jpp.2021.1.03
However, hepcidin may also participate in the pathophysiologic background of hereditary hemochromatosis, anemia of chronic disease, myelodysplastic syndromes or β-thalassemia.
However, hepcidin may also participate in the pathophysiologic background of hereditary hemochromatosis, anemia of chronic disease, myelodysplastic syndromes or β-thalassemia.
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10.1002/hep4.1717
Hereditary hemochromatosis (HH) consists of several inherited disorders that cause inappropriately reduced hepcidin expression in response to body iron stores, leading to increased iron absorption from a normal diet.
Hereditary hemochromatosis (HH) consists of several inherited disorders that cause inappropriately reduced hepcidin expression in response to body iron stores, leading to increased iron absorption from a normal diet.
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10.1159/000513587
Genetic testing confirmed the clinical hypothesis of hereditary hemochromatosis (HH).
Genetic testing confirmed the clinical hypothesis of hereditary hemochromatosis (HH).
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10.3389/fmed.2021.711822
Hereditary hemochromatosis is a genetic iron overload disease related to a mutation within the HFE gene that controls the expression of hepcidin, the master regulator of systemic iron metabolism.
Hereditary hemochromatosis is a genetic iron overload disease related to a mutation within the HFE gene that controls the expression of hepcidin, the master regulator of systemic iron metabolism.
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10.1016/j.clinre.2021.101624
AIM
Hereditary hemochromatosis (HH) is a group of inherited disorders that causes a slow and progressive iron deposition in diverse organs, particularly in the liver.
AIM
Hereditary hemochromatosis (HH) is a group of inherited disorders that causes a slow and progressive iron deposition in diverse organs, particularly in the liver.
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10.1111/apt.16298
In a large collaborative analysis Buch et al1 explored the potential role of genetic variants in conferring susceptibility to develop advanced liver disease in a wide population of individuals with hereditary hemochromatosis (HH).
In a large collaborative analysis Buch et al1 explored the potential role of genetic variants in conferring susceptibility to develop advanced liver disease in a wide population of individuals with hereditary hemochromatosis (HH).
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10.1007/s00289-021-03932-2
Iron overload syndromes can be widely classified as hereditary hemochromatosis.
Iron overload syndromes can be widely classified as hereditary hemochromatosis.
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10.1016/j.bpc.2019.106242
It mediates cellular iron import through a constitutive clathrin-dependent endocytosis mechanism and by recruiting iron- regulator proteins as transferrin, Hereditary Hemochromatosis factor (HFE) and serum ferritin in response to cellular demand.
It mediates cellular iron import through a constitutive clathrin-dependent endocytosis mechanism and by recruiting iron- regulator proteins as transferrin, Hereditary Hemochromatosis factor (HFE) and serum ferritin in response to cellular demand.
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10.1360/tb-2019-0242
Iron overload-related cardiomyopathy is a secondary form of heart disease resulting from iron accumulation in the myocardium and is the leading cause of morbidity in hereditary hemochromatosis, thalassemia major, and other conditions associated with secondary iron overload.
Iron overload-related cardiomyopathy is a secondary form of heart disease resulting from iron accumulation in the myocardium and is the leading cause of morbidity in hereditary hemochromatosis, thalassemia major, and other conditions associated with secondary iron overload.
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10.1182/blood-2018-06-815894
The inability to appropriately regulate hepcidin production in response to these physiologic cues underlies genetic disorders of iron overload and deficiency, including hereditary hemochromatosis and iron-refractory iron deficiency anemia.
The inability to appropriately regulate hepcidin production in response to these physiologic cues underlies genetic disorders of iron overload and deficiency, including hereditary hemochromatosis and iron-refractory iron deficiency anemia.
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10.1093/gerona/gly270
Given the availability of treatment, hereditary hemochromatosis is a strong candidate for precision medicine approaches to improve outcomes in late life.
Given the availability of treatment, hereditary hemochromatosis is a strong candidate for precision medicine approaches to improve outcomes in late life.
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10.15537/smj.2019.9.24482
OBJECTIVES
To evaluate any association between the frequency of hereditary hemochromatosis (HFE) gene mutation (H63D and C282Y) and iron overload in beta-thalassemia major (BTM) patients.
OBJECTIVES
To evaluate any association between the frequency of hereditary hemochromatosis (HFE) gene mutation (H63D and C282Y) and iron overload in beta-thalassemia major (BTM) patients.
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10.1016/j.ymthe.2019.01.003
Here, we utilized ginger NP-derived lipid vectors (GDLVs) in a proof-of-concept investigation to test the hypothesis that inhibiting expression of divalent metal-ion transporter 1 (Dmt1) would attenuate iron loading in a mouse model of hereditary hemochromatosis (HH).
Here, we utilized ginger NP-derived lipid vectors (GDLVs) in a proof-of-concept investigation to test the hypothesis that inhibiting expression of divalent metal-ion transporter 1 (Dmt1) would attenuate iron loading in a mouse model of hereditary hemochromatosis (HH).
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10.17116/patol20198101135
The paper points out the importance of liver biopsy using Perls' reaction for the diagnosis of liver damage with the development of fibrosis, cirrhosis, and cancer as the main cause of death in patients with hereditary hemochromatosis and presents the results of examining liver biopsy specimens in patients with hemochromatosis.
The paper points out the importance of liver biopsy using Perls' reaction for the diagnosis of liver damage with the development of fibrosis, cirrhosis, and cancer as the main cause of death in patients with hereditary hemochromatosis and presents the results of examining liver biopsy specimens in patients with hemochromatosis.
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10.31373/ejtcm/99913
Hereditary hemochromatosis (HH) is a rare genetic disorder, developing secondary to the accumulation of iron in tissues, which may lead to multiple organ failure.
Hereditary hemochromatosis (HH) is a rare genetic disorder, developing secondary to the accumulation of iron in tissues, which may lead to multiple organ failure.
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10.1016/bs.vh.2019.01.005
Dysregulation of hepcidin production contributes to the pathogenesis of many iron disorders: hepcidin deficiency causes iron overload in hereditary hemochromatosis and non-transfused β-thalassemia, whereas overproduction of hepcidin is associated with iron-restricted anemias seen in patients with chronic inflammatory diseases and inherited iron-refractory iron-deficiency anemia.
Dysregulation of hepcidin production contributes to the pathogenesis of many iron disorders: hepcidin deficiency causes iron overload in hereditary hemochromatosis and non-transfused β-thalassemia, whereas overproduction of hepcidin is associated with iron-restricted anemias seen in patients with chronic inflammatory diseases and inherited iron-refractory iron-deficiency anemia.
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10.1111/ijd.14398
Hereditary hemochromatosis is considered an inherited risk factor.
Hereditary hemochromatosis is considered an inherited risk factor.
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10.1016/S0735-1097(19)33098-0
Hereditary hemochromatosis (HH), an autosomal recessive disease caused by HFE gene mutation, results in excessive intestinal iron absorption and iron deposition in multiple organs.
Hereditary hemochromatosis (HH), an autosomal recessive disease caused by HFE gene mutation, results in excessive intestinal iron absorption and iron deposition in multiple organs.
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10.3390/ph12040170
Genetic defects or prolonged inflammatory stimuli results in dysregulation of this axis, which can lead to several disorders including hereditary hemochromatosis and anaemia of chronic disease.
Genetic defects or prolonged inflammatory stimuli results in dysregulation of this axis, which can lead to several disorders including hereditary hemochromatosis and anaemia of chronic disease.
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10.4254/wjh.v11.i2.186
HFE gene controls the iron uptake from gut, particularly in patients with hereditary hemochromatosis (HH).
HFE gene controls the iron uptake from gut, particularly in patients with hereditary hemochromatosis (HH).
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10.1016/bs.vh.2019.01.004
Deregulation of hepcidin expression is a common feature of genetic and acquired iron disorders: in Hereditary Hemochromatosis (HH) and iron-loading anemias low hepcidin causes iron overload, while in Iron Refractory Iron Deficiency Anemia (IRIDA) and anemia of inflammation (AI), high hepcidin levels induce iron-restricted erythropoiesis.
Deregulation of hepcidin expression is a common feature of genetic and acquired iron disorders: in Hereditary Hemochromatosis (HH) and iron-loading anemias low hepcidin causes iron overload, while in Iron Refractory Iron Deficiency Anemia (IRIDA) and anemia of inflammation (AI), high hepcidin levels induce iron-restricted erythropoiesis.
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10.1016/j.patol.2018.08.005
Hereditary hemochromatosis (HH) includes various disorders in iron metabolism producing iron deposits in several organs.
Hereditary hemochromatosis (HH) includes various disorders in iron metabolism producing iron deposits in several organs.
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10.1002/jmri.27023
Cardiac T2* mapping is a noninvasive MRI method that is used to identify myocardial iron accumulation in several iron storage diseases such as hereditary hemochromatosis, sickle cell disease, and β‐thalassemia major.
Cardiac T2* mapping is a noninvasive MRI method that is used to identify myocardial iron accumulation in several iron storage diseases such as hereditary hemochromatosis, sickle cell disease, and β‐thalassemia major.
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10.1039/c9mt00152b
TFN saturates the plasma of individuals with iron-overload diseases such as hereditary hemochromatosis, prompting release of a poorly-defined low-molecular-mass (LMM) iron species called non-transferrin-bound iron (NTBI).
TFN saturates the plasma of individuals with iron-overload diseases such as hereditary hemochromatosis, prompting release of a poorly-defined low-molecular-mass (LMM) iron species called non-transferrin-bound iron (NTBI).
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10.14309/ajg.0000000000000333
Article Title: ACG Clinical Guideline: Hereditary Hemochromatosis.
Article Title: ACG Clinical Guideline: Hereditary Hemochromatosis.
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Keywords related to Hereditary
Hereditary Angio Oedema
Hereditary Transthyretin Mediated
Hereditary Spherocytosis
Hereditary Graph
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Hereditary Neuropathy
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Hereditary Syndromes
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Hereditary Predisposition
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