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Two Sibling sentence examples within year old girl
Febrile neutropenia and acute liver failure secondary to drug toxicity: 2 case reports In a case series, two siblings were described of whom, a 6-year-old girl developed febrile neutropenia during treatment with doxorubicin, vincristine, methotrexate and cisplatin for osteosarcoma of the distal right femur and a 5-year-old boy developed acute liver failure secondary to methotrexate toxicity during treatment with methotrexate for osteoblastic osteosarcoma of the proximal tibia [not all routes and dosages stated; duration of treatment to reaction onset not stated].
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The present case report discusses two siblings, an 11 year old girl and a 6 year old boy, diagnosed as cases of JLS based on family history and clinical-radiological findings.
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Two Sibling sentence examples within whole exome sequencing
Two Sibling sentence examples within year old boy
Two siblings, a 12-year-old boy (in the following indicated with P1) and a 10-year-old girl (in the following indicated with P2), were referred to our neurologic ambulatory because of mild gait disturbances and incoordination.
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Cases: This case series highlights two siblings in a family of 17 children; a 9-year-old boy and his 4-year-old brother.
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Two Sibling sentence examples within Report Two Sibling
Here, we report two siblings with ACOX1 deficiency born to non-consanguineous Japanese parents.
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Here, we report two siblings with compound heterozygous variants in VPS13D but a considerable divergent phenotype highlighting the difficulties of phenotype–genotype correlation in this rare disease.
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Two Sibling sentence examples within Describe Two Sibling
CASE DESCRIPTION
We describe two siblings who presented with similar clinical features including severe intellectual disability and epilepsy with onset of symptom in early infancy.
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We describe two siblings from a consanguineous Turkish family with dysmorphic features, developmental delay, brain malformation, and epilepsy carrying a homozygous mutation (p.
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Two Sibling sentence examples within Present Two Sibling
Two Sibling sentence examples within Identified Two Sibling
We identified two sibling pairs with cystic fibrosis with genetically highly divergent isolates and one pair with closely related isolates, and 25 uninfected presumed household contacts with cystic fibrosis.
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We identified two siblings with COVID orchitis and hypothesized that genetic mutations are associated with susceptibility.
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Two Sibling sentence examples within Least Two Sibling
There was a statistically significant association between diarrhea and age of the child (6–11 and 12–23), poor knowledge of mothers/caretakers on diarrhea prevention methods, families with poor wealth index, being unvaccinated against measles, improper liquid waste disposal, unsafe child feces disposal, and having at least two siblings.
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19 Methods: During the physical examination in Cancer Hospital, Chinese Academy of Medical 20 Sciences, 43,300 people were asked if they have at least two siblings who developed cancer.
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Two Sibling sentence examples within Described Two Sibling
Two Sibling sentence examples within two sibling species
The demographic history of different populations in these two sibling species was reconstructed, and showed that peaks and bottlenecks of effective population size occurred at different times for the two species.
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Two Sibling sentence examples within two sibling pair
Conclusions Here, we report the clinical presentations, neuroimaging and molecular and functional analyses of novel mutations in NDUFV2 in two sibling pairs of two Chinese families presenting with PCL.
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We identified two sibling pairs with cystic fibrosis with genetically highly divergent isolates and one pair with closely related isolates, and 25 uninfected presumed household contacts with cystic fibrosis.
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At the time of diagnosis, the two siblings of the proband were asymptomatic.
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1 The objective of this study is to document the case of two siblings with this condition, from a non-Agrawal Indian community and briefly describe the imaging features of this condition.
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Two siblings also harbored the novel intronic 6Ω pseudoexon GHR variant in compound heterozygosity with the known GHR c.
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The focus was on two sibling musical interactions, based on the recorded soundscape of Anna and her younger brother, Albert.
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Two siblings with the same male unbalanced karyotype demonstrate sex reversal.
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We describe the clinical course in two siblings who developed cardiomyopathy and ventricular fibrillation in infancy.
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We report three patients, including two siblings, with HLCSD and significant cutaneous manifestations including ichthyosiform dermatitis and a presentation with features of annular pustular psoriasis.
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Our report of HSOS during chemotherapy treatment in two siblings with AT calls for additional precautions to reduce the intensity of chemotherapy and use HSOS prophylaxis in similar cases.
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All four patients (two siblings and their cousins, from a pedigree described previously) had the heterozygous S163R mutation.
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We report on two siblings suffering from different pathogenic conditions, born to consanguineous parents.
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All three had redundant and doughy‐textured skin and two siblings from one family had facial dysmorphism.
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We described three cases, two siblings and their cousin, affected by ANE, all of them exhibiting RAN-binding protein 2 (RANBP2) gene mutation.
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Examination showed proximal muscle weakness of the upper and lower extremities and hyperlaxity of the wrist and fingers in both with some variability in clinical severity noted between the two siblings.
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MATERIAL AND METHODS
Two siblings with CTX aged 40 and 38 years, respectively, who had been diagnosed with CTX for 16 years were enrolled.
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Here, we provide a detailed clinical and molecular characterization of two siblings with microcephaly, developmental delay, cerebellar volume loss, hypomyelination, with cardiac conduction and rhythm abnormalities including sinus node dysfunction, intraventricular conduction delay, atrioventricular block, and ventricular tachycardia (VT) due to compound heterozygous variants in EXOSC5: (1) NM_020158.
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The first family, 491, had six members with features of CS, including two siblings who presented with presacral, Grade 2 NETs, one of which had metastasized to bone and lymph nodes.
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In this study we demonstrate the existence of two sibling species within the C.
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Two siblings (III-2 and III-5) developed bouts of laughing and crying leading to apneic spells.
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Correspondingly, compared with women with no siblings those women with three siblings or more had an increased risk of cardiovascular events, and those with two siblings or more had an increased risk of coronary events.
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Here, we present the case of two siblings with IPEX syndrome with the same hemizygous mutation, but with different types of symptomology at onset of the disease.
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Herein, we report the therapeutic effects of dietary therapy, cysteamine, and NAC in two siblings with ECHS1D, including their clinical, neuroradiological, and chemical aspects.
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Methods and Results In this study, we report an family with two siblings exhibiting two different NMD, Miyoshi muscular dystrophy (MMD) and early onset primary dystonia (EOPD).
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METHODS
Case report of two siblings.
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The child lived with her parents and two siblings.
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Conclusions Here, we report the clinical presentations, neuroimaging and molecular and functional analyses of novel mutations in NDUFV2 in two sibling pairs of two Chinese families presenting with PCL.
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The authors provide a review of the breadth of mutations within the ACTA2 literature and report a case of two siblings with de novo ACTA2 Arg258Cys mutations with differing clinical courses, highlighting the utility of indirect revascularization with 8-year follow-up data.
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A balanced translocation was found in two siblings diagnosed with azoospermia.
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Two siblings were studied; in one of the siblings, maternally originated 17q12 duplication was identified, and paternally originated 16p11.
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Case presentation In this case report, we describe the clinical and biochemical characteristics of two siblings with LS, a sister and a brother, and identify a homozygous c.
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In this report, we describe a Sicilian family with two siblings affected with congenital coloboma, microphthalmia, and a mild delay of motor developmental milestones.
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Until now, only one study reported FAR1 deficiency in two families with three affected children (two siblings homozygous for c.
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1 as the core of the synergy and shared by two sibling introgression lines in IR64 genetic background, i.
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This case of CD in two siblings, male and female, highlights the unique stress experienced by each patient at the time of symptom onset, the severity of their inflammatory symptoms, and their course of disease over several years.
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Two siblings with TT1 and acute liver dysfunction were diagnosed with hyperinsulinaemic hypoglycaemia in the neonatal period.
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METHODS
The clinical data and mutations in ADCK4 of two siblings with steroid-resistant NS were collected.
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Two sibling bare-backed bat species (Pteronotus fulvus and P.
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Two siblings present with early lethal noncompaction cardiomyopathy (NCCM).
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We here describe the identification of a novel variant in the anti‐inflammatory Annexin A1 protein likely to be the cause of disease in two siblings with autosomal recessive parkinsonism.
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HSCT using non‐TBI based conditioning was performed on two siblings with FA.
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We report here two siblings from a large Ashkenazi Jewish family, presenting with a progressive neuromuscular disease characterized by ataxia and myopathy.
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While a few cases of Philemon and Baucis deaths involving couples of spouses have been reported in the literature, only one paper describes the simultaneous deaths of two siblings.
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The demographic history of different populations in these two sibling species was reconstructed, and showed that peaks and bottlenecks of effective population size occurred at different times for the two species.
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The scoliosis found in two siblings has not been associated with protein O-mannosyltransferase 2 gene mutations related to limb-girdle muscular dystrophy 2N in previous reports.
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Two sibling species of Anisakis are found in S.
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OBJECTIVE
Two siblings born to a Turkish family of consanguineous marriage had mixed neurological presentations with the presence of hypointense images on T2-weighted MRI and were pre-diagnosed as having autosomal recessive spastic paraparesis or ataxia.
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We herein report a novel SZT2 variant in one of two siblings both diagnosed with epilepsy of infancy with migrating focal seizures (EIMFS).
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We report on two siblings with ML III γ bearing the previously undescribed c.
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We observed in two siblings with early-onset age (< 45) and autopsy confirmed DLB, compound heterozygous missense mutations in VPS13C , p.
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