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Results 1 - 10 of 16 for Congenital diarrhea 6
  1. Microvillus inclusion disease 
    ... atrophy with diarrhea 2 MVID Genetic Testing ... inclusion disease: a clinicopathologic study of 17 cases from the UK. Ultrastruct Pathol. 2010 Dec;34(6):327-32. doi: 10.3109/01913123.2010.500447. ...
    https://medlineplus.gov/.../condition/microvillus-inclusion-disease - Genetics
  2. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome 
    ... syndromes. Autoimmunity-immunodeficiency syndrome, X-linked Diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea Diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked Enteropathy, ...
    https://medlineplus.gov/...ocrinopathy-enteropathy-x-linked-syndrome - Genetics
  3. Familial candidiasis 
    ... Glocker E, Grimbacher B. Chronic mucocutaneous candidiasis and congenital susceptibility to Candida. Curr Opin Allergy Clin Immunol. 2010 Dec;10(6):542-50. doi: 10.1097/ACI.0b013e32833fd74f. Citation ...
    https://medlineplus.gov/genetics/condition/familial-candidiasis - Genetics
  4. Congenital sucrase-isomaltase deficiency 
    ... Zimmer KP, Schmitz J, Jacob R, Naim HY. Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum. Gastroenterology. 2003 Dec;125(6):1678-85. doi: 10.1053/j.gastro.2003. ...
    https://medlineplus.gov/.../congenital-sucrase-isomaltase-deficiency - Genetics
  5. Lactose intolerance 
    ... non-genetic causes.Congenital lactase deficiency, also called congenital alactasia, is a disorder in which infants are unable to break down the lactose in breast milk or formula. This form of lactose intolerance results in very severe diarrhea. If affected infants are not given a lactose- ...
    https://medlineplus.gov/genetics/condition/lactose-intolerance - Genetics
  6. TCN2 gene 
    ... 1007/s10545-010-9145-z. Epub 2010 Jul 6. Citation on PubMed Qian L, Quadros EV, Regec A, Zittoun J, Rothenberg SP. Congenital transcobalamin II deficiency due to errors in RNA ...
    https://medlineplus.gov/genetics/gene/tcn2 - Genetics
  7. Porphyria 
    ... PORPHYRIA; VP PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED; XLEPP PORPHYRIA, CONGENITAL ... diagnosis and treatment of the acute porphyrias. Ann Intern Med. 2005 Mar 15;142(6):439-50. doi: 10.7326/0003-4819-142- ...
    https://medlineplus.gov/genetics/condition/porphyria -
  8. Abetalipoproteinemia 
    ... Kornzweig disease Bassen-Kornzweig syndrome Betalipoprotein deficiency disease Congenital betalipoprotein deficiency syndrome Microsomal ... disorders and apolipoprotein B metabolism. Crit Rev Clin Lab Sci. 2005;42(5-6):515-45. doi: 10.1080/10408360500295113. Citation on ...
    https://medlineplus.gov/genetics/condition/abetalipoproteinemia - Genetics
  9. Glucose-galactose malabsorption 
    ... glucose and galactose, which primarily results in severe diarrhea. Beginning in infancy, severe diarrhea results in weight loss and dehydration that can ...
    https://medlineplus.gov/.../glucose-galactose-malabsorption - Genetics
  10. Tyrosinemia 
    ... thrive) because eating high-protein foods leads to diarrhea and vomiting. Affected infants may also have yellowing ... long-term outcome. Pediatr Int. 2011 Dec;53(6):985-9. doi: 10.1111/j.1442-200X. ...
    https://medlineplus.gov/genetics/condition/tyrosinemia - Genetics
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