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19 Possible Causes for Congenital Watery Diarrhea

  • Congenital Chloride Diarrhea

    Infrequency of congenital chloride diarrhea makes diagnostics difficult.[ncbi.nlm.nih.gov] The clinical presentation is a life-threatening watery diarrhea with a high chloride content.[ncbi.nlm.nih.gov] Abstract Congenital chloride diarrhea (CLD) is characterized by watery stools with high chloride content beginning prenatally and is inherited as an autosomal recessive trait[ncbi.nlm.nih.gov]

  • Cholestasis

    The initial symptoms associated with PFIC may be foul smelling, greasy stools or watery diarrhea, which are often present at birth (congenital).[rarediseases.org]

  • Congenital Lactase Deficiency

    Congenital lactase deficiency is a severe gastrointestinal disorder characterized by watery diarrhea in infants fed with breast milk or other lactose-containing formulas.[ncbi.nlm.nih.gov] Abstract Congenital lactase deficiency (CLD) is a severe gastrointestinal disorder characterized by watery diarrhea in infants fed with breast milk or other lactose-containing[ncbi.nlm.nih.gov] Abstract Congenital lactase deficiency (CLD) is an autosomal recessive, gastrointestinal disorder characterized by watery diarrhea starting during the first 1-10 d of life[ncbi.nlm.nih.gov]

  • Arthrogryposis-Renal Dysfunction-Cholestasis Syndrome

    The initial symptoms associated with PFIC may be foul smelling, greasy stools or watery diarrhea, which are often present at birth (congenital).[rarediseases.org]

  • Intestinal Lymphangiectasia

    […] at age 83 with symptoms of watery diarrhea, abdominal distention, 5-Kg-weight-gain, and weakness for one month, and had typical clinical findings of PIL including chylous[ncbi.nlm.nih.gov] RATIONALE: Primary intestinal lymphangiectasia (PIL) is a rare, presumably congenital lesion that is usually diagnosed in patients DIAGNOSES: A patient initially presented[ncbi.nlm.nih.gov]

  • Congenital Sucrase-Isomaltase Deficiency

    In each infant watery diarrhea occurred and persisted for many months, and it was assumed that the original gastrointestinal disorder was responsible.[ncbi.nlm.nih.gov] It belongs to the heterogeneous group of congenital diarrheal disorders and typically manifests within the first year of a child's life in form of persistent watery diarrhea[symptoma.com] In three infants the formula had been prescribed for presumed postgastroenteritis diarrhea, and in a fourth it was begun after resection of a short-segment congenital ileal[ncbi.nlm.nih.gov]

  • Protein Losing Enteropathy

    Homepage Rare diseases Search Search for a rare disease Congenital chronic diarrhea with protein-losing enteropathy Disease definition Congenital chronic diarrhea with protein-losing[orpha.net] […] enteropathy is a rare, genetic, intestinal disease characterized by early-onset, chronic, non-infectious, non-bloody, watery diarrhea associated with protein-losing enteropathy[orpha.net]

  • Congenital Malabsorption of Folic Acid

    watery diarrhea Congenital glucose-galactose malabsorption Acidic diarrhea Congenital lactase deficiency Acidic diarrhea Congenital chloride diarrhea Hydramnion, secretory[clinicalgate.com] watery diarrhea Metabolic alkalosis Congenital defective jejunal Na /H exchange Hydramnion, secretory watery diarrhea Congenital bile acid malabsorption Steatorrhea Congenital[clinicalgate.com] In secretory diarrhea due to disorders such as congenital chloride diarrhea and microvillus inclusion disease, the stool is watery and voluminous and can be mistaken for urine[clinicalgate.com]

  • Disaccharidase Deficiency

    […] feeding, which causes explosive, watery, frothy stools and abdominal distention Acquired deficiency: Common in North American blacks Causes osmotic diarrhea Acquired deficiency[pathologyoutlines.com] Definition / general Disaccharidases are located in apical cell membrane of villous absorptive epithelial cells Congenital deficiency: Rare; malabsorption evident with milk[pathologyoutlines.com]

  • Intrahepatic Cholestasis

    The initial symptoms associated with PFIC may be foul smelling, greasy stools or watery diarrhea, which are often present at birth (congenital).[rarediseases.org]

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