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3,563 Possible Causes for Autosomal Dominant, Obesity, Pediatric Disorder

  • Pseudohypoparathyroidism

    Obesity may be because of a decrease in resting energy expenditure because most patients do not report significant hyperphagia.[journals.lww.com] Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism . 4th ed.[pedsinreview.aappublications.org] PHP-Ib familial form, with an autosomal dominant pattern of transmission (autosomal dominant pseudohypoparathyroidism type Ib [AD-PHP-Ib]), is typically characterized by an[ncbi.nlm.nih.gov]

  • Kallmann Syndrome

    Patients with this genetic form of KS have been reported to have a possible increased prevalence of obesity and sleep disorders, which may be related to the role of PROK2[ncbi.nlm.nih.gov] Developmental disorders with olfactory abnormalities, developmental lag, heart malformations, external genital malformations.[ncbi.nlm.nih.gov] Kallmann syndrome characterised by hypogonadotropic hypogonadism (HH) and anosmia is genetically heterogeneous with X-linked, autosomal dominant and autosomal recessive forms[ncbi.nlm.nih.gov]

  • CHARGE Syndrome

    , polydactyly, and intellectual disabilities) 759.89 Barth 759.89 basal cell nevus 759.89 Beckwith (-Wiedemann) 759.89 Biedl-Bardet (obesity, polydactyly, and intellectual[icd9data.com] She is a specialist in pediatric communication disorders and augmentative communication.[smartspeechtherapy.com] CHARGE syndrome is an autosomal dominant condition caused by mutations in chromodomain helicase DNA-binding 7.[ncbi.nlm.nih.gov]

  • Familial Partial Lipodystrophy

    In the present study we aimed to identify cases of FPLD among non-obese patients with type 2 diabetes mellitus and marked insulin resistance.[ncbi.nlm.nih.gov] , including general internists, pediatric and adult endocrinologists, pediatricians, lipidologists, cardiologists, internists, and geneticists.[books.google.com] Autosomal dominant familial partial lipodystrophy (FPLD) due to mutant LMNA encoding nuclear lamin A/C is characterized by adipose tissue repartitioning together with multiple[ncbi.nlm.nih.gov]

  • Pseudopseudohypoparathyroidism

    obese.[doi.org] Germany J Pediatr 150:618-22, 622.e1-5. 2007 ..To analyze the frequencies and clinical presentation of definable somatic disorders in children who are overweight...[labome.org] Pseudopseudohypoparathyroidism is a very rare autosomal dominant genetic disorder that is considered to be a variant of Albright's hereditary osteodystrophy.[symptoma.com]

  • Depression

    […] depression to have obesity. 8 Cancer.[womenshealth.gov] [Pediatr Ann. 2018;47(7):e261-e265.]. Copyright 2018, SLACK Incorporated.[ncbi.nlm.nih.gov] Neuroimaging of her brain suggested pathological changes out of keeping with her age, leading to further investigations including genetic testing for cerebral autosomal dominant[ncbi.nlm.nih.gov]

  • Williams-Beuren Syndrome

    […] mouth Feeding problems Irritability in infancy and prolonged colic Difficulty with transitions from bottle feeding to solids Difficulty gaining weight in infancy followed by obesity[stlouischildrens.org] Pediatric Feeding Disorders Program - Provides assessment and treatment for children who have difficulty eating related to food selectivity, food refusal, and disruptive mealtime[urmc.rochester.edu] Williams-Beuren syndrome is an autosomal dominant disorder resulting from a submicroscopic deletion of contiguous genes on the long arm of chromosome 7.[ncbi.nlm.nih.gov]

  • Vitamin D Deficiency

    Trial, Obesity, 26, 4, (651-657), (2018).[doi.org] Hypocalcemic and hypercalcemic disorders in children . Current Problems in Pediatrics, Vol. 19, Issue. 10, p. 497. CrossRef Google Scholar Poskitt, E.M.E. 1988.[doi.org] dominant or X-linked hypophosphatemic rickets c 1,25(OH) 2 D levels are usually normal for patients taking the medications listed, and those with nephrotic syndrome, hepatic[questdiagnostics.com]

  • Klinefelter Syndrome

    Obesity is reported to have adverse effects on semen quality and the endocrine system.[ncbi.nlm.nih.gov] disorders, resulting in a rise in the diagnosis and early referral to the pediatric endocrinologist.[ncbi.nlm.nih.gov] Neurofibromatosis is an autosomal dominant disorder characterized by cafe-au-lait spots and fibromatous tumors of the skin.[ncbi.nlm.nih.gov]

  • Hyperlipoproteinemia Type 3

    Hypothyroidism, obesity, or diabetes can make the condition worse.[medlineplus.gov] […] recessive or autosomal dominant condition (that is, if the trait has been inherited from both parents).[britannica.com] […] these symptoms Corneal arcus 0001084 Diabetes mellitus 0000819 Hepatic steatosis Fatty infiltration of liver Fatty liver [ more ] 0001397 Hepatomegaly Enlarged liver 0002240 Obesity[rarediseases.info.nih.gov]

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