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6,334 Possible Causes for Mutation in the VPS53 Gene, Pediatric Disorder

  • Acute Gastroenteritis

    Seventy children with acute gastroenteritis and their parents completed the Rome III Diagnostic Questionnaire for Pediatric Functional GI Disorders and the Children's Somatization[ncbi.nlm.nih.gov] Rotavirus gastroenteritis: precursor of functional gastrointestinal disorders?. J Pediatr Gastroenterol Nutr . 2009 Nov. 49(5):580-3. [Medline] .[emedicine.medscape.com] Use of probiotics in childhood gastrointestinal disorders. J Pediatr Gastroenterol Nutr 1998;27:323--32. Guandalini S, Pensabene L, Zikri MA, et al.[cdc.gov]

    Missing: Mutation in the VPS53 Gene
  • Vitamin D Deficiency

    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]

    Missing: Mutation in the VPS53 Gene
  • Acute Alcohol Intoxication

    The inactive ALDH2(2) allele is dominant , J Clin Invest , 1989 , vol. 83 (pg. 314 - 6 ) Diagnostic and Statistical Manual of Mental Disorders , 2000 4th ed Washington, DC[academic.oup.com] American Psychiatry Association Text Revision Estimated blood alcohol concentrations for child and adolescent drinking and their implications for screening instruments , Pediatrics[academic.oup.com]

    Missing: Mutation in the VPS53 Gene
  • Constipation

    Mousa, The value of fluoroscopic defecography in the diagnostic and therapeutic management of defecation disorders in children, Pediatric Radiology, 45, 2, (173), (2015).[doi.org] Major symptoms and signs of digestive tract disorders. In: Kliegman RM, Stanton BF, St. Geme JW, Schor NF, eds. Nelson Textbook of Pediatrics. 20th ed.[medlineplus.gov]

    Missing: Mutation in the VPS53 Gene
  • Valinemia

    PCH2E ( OMIM ) is caused by mutation in the VPS53 gene ( OMIM ) on chromosome 17p13. PCH2F ( OMIM ) is caused by mutation in the TSEN15 gene ( OMIM ) on chromosome 1q25.[mendelian.co] PCH2D ( OMIM ) is caused by mutation in the SEPSECS gene ( OMIM ) on chromosome 4p15.[mendelian.co] […] in the TSEN34 gene ( OMIM ) on chromosome 19q13.[mendelian.co]

  • Urinary Tract Infection

    A urinary tract infection (UTI) is an infection that affects part of the urinary tract. When it affects the lower urinary tract it is known as a bladder infection (cystitis) and when it affects the upper urinary tract it is known as a kidney infection (pyelonephritis). Symptoms from a lower urinary tract infection[…][en.wikipedia.org]

    Missing: Mutation in the VPS53 Gene
  • Anemia

    One of the most common pediatric disorders, anemia has many potential causes. Anemia is often a symptom of a disease rather than a disease itself.[childrenshospital.org] In addition to an experienced, compassionate nurse coordinator (who provides your child and family support, education and care coordination), Nemours’ pediatric blood disorder[nemours.org] How can I manage anemia if my child has an inherited red blood cell disorder?[healthychildren.org]

    Missing: Mutation in the VPS53 Gene
  • Depression

    [Pediatr Ann. 2018;47(7):e261-e265.]. Copyright 2018, SLACK Incorporated.[ncbi.nlm.nih.gov] This includes serious adult psychiatric illnesses such as major depressive disorder, anxiety disorders, and substance abuse.[ncbi.nlm.nih.gov]

    Missing: Mutation in the VPS53 Gene
  • Acne Vulgaris

    Tollefson, Endocrine disorders and hormonal therapy for adolescent acne, Current Opinion in Pediatrics, 10.1097/MOP.0000000000000515, 29, 4, (455-465), (2017).[doi.org] Consensus statement on management of intersex disorders. J Pediatr Urol 2006 ; 2: 148 62 Google Scholar Crossref Medline 55. Hughes, IA.[doi.org] Read More Pediatric Dermatology Corrective Camouflage in Pediatric Dermatology Author: Tedeschi A Dall'oglio F Micali G Schwartz RA Janniger CK Many dermatologic diseases,[mdedge.com]

    Missing: Mutation in the VPS53 Gene
  • Hypoglycemia

    Abstract CHARGE syndrome is a rare autosomal dominant disorder involving multiple organs.[ncbi.nlm.nih.gov] Pediatrics 1990;85:834-837. Cornblath M, Schwartz R. Disorders of Carbohydrate Metabolism in Infancy. 3rd ed. Philadelphia: W.B. Saunders, 1991, pp. 87-124, 225-246.[uichildrens.org] Forsyth, “Unifying the definitions of sudden unexpected death in epilepsy”: A pediatric perspective, Epilepsia, 53, 6, (1109-1110), (2012).[doi.org]

    Missing: Mutation in the VPS53 Gene

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