Introduction to Child Diagnosed

What is/are Child Diagnosed?

Child Diagnosed - The empirical data consists of a longitudinal semi-structured observation of a child diagnosed with autistic spectrum disorder. ^[1] The theme has social relevance, since the child diagnosed with autism is labeled and stigmatized, seen as a student who has a "problem" and will not learn. ^[2] Background Currently, there is limited research on how having a child diagnosed with achondroplasia affects parents’ lives. ^[3] Here we present the case of a child diagnosed with primary hyperoxaluria type 1 after kidney transplant who was able to maintain kidney function, thanks to aggressive renal replacement therapy as well as initiation of a new targeted therapy for this disease. ^[4] 8 In this case report, we report a child diagnosed with an anterior transolecranon fracture dislocation with an associated avulsion fracture of the coronoid process of the ulna. ^[5] Background Having a child diagnosed with cancer is a devastating experience that may affect parents’ mental health. ^[6] Encountering a child diagnosed with SLE at a very young age, pediatricians should consider immunodeficiency syndrome including DOCK8 deficiency. ^[7] This approach also offers a response to the mother of a child diagnosed as autistic weeks after a measles vaccine – who refuses to accept robust statistical evidence that the vaccine did not cause the disease. ^[8] We report the case of a child diagnosed with MPS I who presented with overt stroke and repeated neurological symptoms with imaging findings for severe ventriculomegaly, infarction, and bilateral terminal carotid artery stenosis. ^[9] e18722 Background: Caring for a child diagnosed with cancer may adversely affect mental health (MH) of parents. ^[10] Objective Evaluation of a clinical case of hematologic malignancy in a child diagnosed with primary immunodeficiency WAS. ^[11] We report a case of endobronchial pulmonary actinomycosis in a child diagnosed on endobronchial biopsy and broncho-alveolar lavage taken during bronchoscopy. ^[12] Method: Observational case study (before and after), descriptive and exploratory, with a child diagnosed with ASD. ^[13] Materials and Methods  Consenting parents accompanying children to therapeutic programs in selected institutions were administered a semi structured interview schedule incorporating questions of the vernacular version of the Perceived Stress Scale (PSS-10), emotion-based coping strategies, spousal support in care of the child diagnosed with ASD, and possible-associated factors. ^[14] Objective: This qualitative study explored the experiences of mothers who had a child diagnosed with cancer. ^[15] Background: Raising a child diagnosed with cerebral palsy (CP) is a major challenge for parents and may greatly change the family’s lifestyle. ^[16] When a child diagnosed with ASD lives in a bilingual environment, the parents often express concerns about whether their child should learn both languages simultaneously, turning to specialists for advice. ^[17] BACKGROUND Parenting a child diagnosed with intellectual disability includes a variety of stressors. ^[18] The case of a child diagnosed with Burkitt leukemia developing chemotherapy-induced oral mucositis in home care is presented to show the therapeutic impact of early symptom detection with a daily web-based tool. ^[19] The nature of this study is to bring out the incongruent gender identity of the child diagnosed with gender dysphoria. ^[20] 27 (before and after) for child diagnosed depression and 0. ^[21] This study reports parent expectations and experiences when having a child diagnosed with ASD in preschool. ^[22] One of the most difficult aspects of being parents of a child diagnosed with cancer is to balance normal family life with the sick child’s needs and treatment requirements. ^[23] Case A: The child diagnosed with AML, was admitted to the hospital. ^[24] OBJECTIVE To analyze the clinical phenotype and pathogenic variant in a child diagnosed with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH). ^[25] This study was conducted to investigate the effectiveness of the Family Empowerment Program, which aims to reduce the stress level of parents with a child diagnosed with Attention Deficit Hyperactivity Disorder (ADHD) and to increase their quality of life. ^[26] We report a case of endobronchial actinomycosis in a child diagnosed on endobronchial biopsy and bronchoalveolar lavage (BAL). ^[27] The purpose of this study is to assess the effect of Clinutren Junior high-calorie formula for children from 1 to 10 years of age on the growth and development of the child diagnosed with type I spinal muscular atrophy. ^[28] Here we describe a child diagnosed with SRY‐negative 46,XX OT‐DSD after completing a series of complex clinical genetic analyses, including chromosomal microarray, DSD gene panel (sequencing and deletion/duplication analysis), whole exome sequencing, and whole genome sequencing. ^[29] For each child diagnosed with FED, 10 age- and sex-matched controls who did not meet the criteria for FED were randomly selected from the general population. ^[30] Having a child diagnosed with cancer is stressful for the whole family and may cause significant psychological impact on parents and siblings. ^[31] METHOD : This is a case study realized with a child diagnosed with SRT, evaluated before, during, and after physiotherapy sessions, through the Alberta Infant Motor Scale. ^[32] Participation in tourism is lower among families with a child diagnosed with Autism Spectrum Disorder than among comparable families. ^[33] Here, we describe another rare case of parotid lipoma in a child diagnosed preoperatively by magnetic resonance imaging (MRI) and ultrasonography (US). ^[34] In our study, we present the case of a child diagnosed with both autism spectrum disorder and attention deficit/hyperactivity disorder, who developed bilateral gynecomastia in association with continuous methylphenidate monotherapy for 6 months. ^[35] However, there was no significant association between repeat length and having a child diagnosed with an IDD condition. ^[36] Although management of a child diagnosed with concomitant occurrence of trisomy 10p and terminal 14q deletion by a multidisciplinary approach emphasizing physiotherapeutic intervention has shown remarkable improvement in motor skills, the care of children diagnosed with these genetic aberrations needs further investigation. ^[37] Maternal FoP was significantly associated with depression, a medical coping style, a child diagnosed with a CNS tumor in comparison to leukemia, and lower family functioning (adjusted R2 =. ^[38] Prior to the discover of insulin, a child diagnosed with diabetes had an average life expectancy of only a matter of months. ^[39] OBJECTIVE Parents are the main caregivers when there is a child diagnosed with cancer. ^[40] 2–7 Here we describe the clinical course of a child diagnosed with primary hepatic Burkitt lymphoma (PHBL). ^[41] We report a case of a child diagnosed with PCH without an intracranial disease. ^[42] DESIGN AND METHODS This research work used a phenomenological approach with the interview of a purposeful sample of eleven mothers having a child diagnosed with T1D. ^[43] For the definition of the sample, the following inclusion criteria were listed: being a mother of a child diagnosed with microcephaly due to Zika Virus, having given birth, and being a resident of the municipality of Mossoro, Rio Grande do Norte, Brazil. ^[44] One factor related to family burden, which has been examined in previous studies, involves the interaction of the parent with the child diagnosed with the disorder. ^[45]

8 year old

We present a case of an 8-year-old male child diagnosed with Crohn's disease, and he experienced a steroid-induced psychosis during induction of remission with corticosteroid therapy. ^[1] We present a case of broma present on the palatal region in an 8- year-old child diagnosed based on clinical, radiological, and histological features. ^[2] We report a new case of vulvar wart in an 8-year-old child diagnosed initially as hymeneal polyps. ^[3]

year old male

A 4 year old male child diagnosed with spastic cerebral palsy’s, pre and post treatment measures, data of Modified Ashworth Scale, Pediatric Manual Muscle Testing and Gross Motor Function-66 were evaluated and mentioned. ^[1]

Old Child Diagnosed

The present case report describes the unique management, 5-year follow-up, and prognosis of a 10-year-old child diagnosed with lateral luxation and horizontal apical root fracture of maxillary central incisor with open apex. ^[1] Design: In this single-center, phase 2, parallel, 1:1:1 randomized trial conducted December 2016 to December 2018, English-speaking parents with a 2-24 year-old child diagnosed with new cancer were randomly assigned to UC, one-on-one, or group PRISM-P, a brief, skill-based curriculum targeting stress management, goal setting, cognitive reframing, and meaning making. ^[2] The current report highlights a unique case of a 3-year-old child diagnosed with adrenal NBL metastasizing to the mandible and the dura. ^[3] We present a case of broma present on the palatal region in an 8- year-old child diagnosed based on clinical, radiological, and histological features. ^[4] The research conducted with a five-year-old child diagnosed with childhood autism evaluates the effectiveness of using of a token economy reinforcer system and discrete trial teaching method for establishing matching and discrimination skills (animal discrimination and matching identical stimuli), as well as answering yes/no questions about preferred items. ^[5] We report a new case of vulvar wart in an 8-year-old child diagnosed initially as hymeneal polyps. ^[6] We present the case of a 6 years old child diagnosed with tuberculous meningitis based on epidemiological, clinical and biological data and who has rapidly developed neurological complications with persistent fever and headache for a long time. ^[7] 3 Sirolimus was first reported to be used in RDD by Cooper et al, wherein a 20-month-old child diagnosed with RDD continued to have multiple autoimmune manifestations that were refractory to other drugs. ^[8] We present a 4‐year‐old child diagnosed with an autistic spectrum disorder and global developmental delay, limiting his communication skills. ^[9] The subjects were a 5-year-old child diagnosed with bronchopulmonary dysplasia. ^[10] In the current paper, we are presenting the case of an 11-year-old child diagnosed in our ENT Department with congenital anosmia. ^[11]

Male Child Diagnosed

A 4 year old male child diagnosed with spastic cerebral palsy’s, pre and post treatment measures, data of Modified Ashworth Scale, Pediatric Manual Muscle Testing and Gross Motor Function-66 were evaluated and mentioned. ^[1] Methods: DNA from a male child diagnosed as having X-HIGM and DNA from his healthy mother were used for whole-exome (next-generation) sequencing and targeted gene sequencing. ^[2] We present a case of an 8-year-old male child diagnosed with Crohn's disease, and he experienced a steroid-induced psychosis during induction of remission with corticosteroid therapy. ^[3] Here we report on a male child diagnosed with ASD, showing cognitive and motor impairments, stereotypies, hyperactivity, sleep, and gastrointestinal disturbances. ^[4] Here we report a male child diagnosed as ODCD with a novel compound heterozygote mutation who presented with skeletal changes, short stature, dentinogenesis imperfecta, and facial dysmorphism resembling Achondroplasia (ACH) and Hypochondroplasia (HCH). ^[5] We report a 13-month-old male child diagnosed with PTLD, treatment of which lead to recurrent intestinal perforations. ^[6] This paper looks at a male child diagnosed with cerebral palsy, psychomotor affectation, left spastic hemiparesis, and bilateral sensorineural hearing loss after fetal distress due to ruptured membranes before the delivery of more than 30 hours of evolution and several episodes of severe hypoglycemia. ^[7] Herein, the case of an 8-year-old male child diagnosed with an extremely rare anatomical presentation of a single origin of both the left and right coronary arteries from the non-coronary sinus is presented. ^[8] Determination of the etiology of CTPV may also give a direction toward the management plan to not only relieve the patient of the already developed complications but also to treat the primary cause of the pathology We discuss a case of a nine-year-old male child diagnosed as CTPV secondary to protein C and antithrombin III deficiency who was treated symptomatically for anemia and varices and was referred for transjugular intrahepatic portosystemic shunt (TIPS). ^[9] Our case was a male child diagnosed with AMML at 18 months of age, who presented with hyperleucocytosis, a mild thrombocytopenia and hepato-splenomegaly (Table I). ^[10]

One Child Diagnosed

This present paper reports a phenotypical and laboratory description of two children diagnosed with WAS and one child diagnosed with XLT. ^[1] One child diagnosed with posterior urethral valve (PUV) had mutation in two different genes [TNXB (p. ^[2] Medical, educational, and speech-language documentation of one child diagnosed with AE at age 7 years was reviewed. ^[3] METHODS Study participants were recruited and screened to meet the following inclusion criteria: African-American or Latinx race/ethnicity, household income at or below 185% of the federal poverty line, and at least one child diagnosed with asthma with symptom frequency consistent with uncontrolled asthma according to national guidelines. ^[4] Methods: Participants were mother‐child pairs from MARBLES, a high‐risk pregnancy cohort that enrolls families who have one child diagnosed with ASD and are planning to have another child. ^[5] Unfortunately, one child diagnosed with complete transposition of great arteries combined with interruption of aortic arch (type A) died 5 days after operation due to postoperative low cardiac output syndrome. ^[6]

Young Child Diagnosed

We present the case of a young child diagnosed with stroke secondary to osteosarcoma embolism to the left internal carotid artery and review the relevant literature to discuss the considerations and challenges of treatment of stroke in the pediatric population. ^[1] This paper aims to offer a demonstration of applying general case instruction to teach a young child diagnosed with ASD to request help only when needed while concurrently increasing the child’s independence in task completion. ^[2] Case presentationHere, we report a Chinese young child diagnosed as PFIC with variants in tight junction protein 2 (TJP2). ^[3] Method The experiences and support needs of 13 mothers and fathers who had a young child diagnosed ( Results Thematic analysis identified four key themes: emotional response to diagnosis, ability to manage the uncertainty post-diagnosis, resourcefulness, and experiences of sharing the diagnosis. ^[4]

Female Child Diagnosed

A four-year-old female child diagnosed as a case of severe Seasonal Hyperacute Panuveitis (SHAPU) underwent lens-sparing core vitrectomy in her left eye with intravitreal antibiotic and steroid. ^[1] ANAESTH, PAIN & INTENSIVE CARE; VOL 23(2) JUNE 2019 4 month old female child diagnosed a case of long QT syndrome with recurrent polymorphic ventricular tachycardia (VT) storm with moderate left ventricular (LV) dysfunction with status epilepticus presented with recurrent seizures in an emergency. ^[2]

Age Child Diagnosed

We present the case of a school-age child diagnosed with acute viral myositis. ^[1]