Congenital familial protracted diarrhea with enterocyte brush-border abnormalities

Introduction: Congenital familial protracted diarrhea with enterocyte brush-border abnormalities

Description of Congenital familial protracted diarrhea with enterocyte brush-border abnormalities

Congenital familial protracted diarrhea with enterocyte brush-border abnormalities (medical condition): A rare, inherited, progressive intestinal disease where a defect in the intestinal wall results in severe diarrhea after birth.

See also:

Microvillus Inclusion Disease:
  »Introduction: Microvillus Inclusion Disease
  »Symptoms of Microvillus Inclusion Disease

Congenital familial protracted diarrhea with enterocyte brush-border abnormalities: Related Topics

These medical condition or symptom topics may be relevant to medical information for Congenital familial protracted diarrhea with enterocyte brush-border abnormalities:

• Brush-border
• Congenital
• Congenital disease
• Congenital disorder
• Familial
• Familial disorder
• Diarrhea (2248 causes)
• Enterocyte
• Brush
• Border

Congenital familial protracted diarrhea with enterocyte brush-border abnormalities: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Congenital familial protracted diarrhea with enterocyte brush-border abnormalities is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Congenital familial protracted diarrhea with enterocyte brush-border abnormalities, or a subtype of Congenital familial protracted diarrhea with enterocyte brush-border abnormalities, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Congenital familial protracted diarrhea with enterocyte brush-border abnormalities as a "rare disease".

Source - Orphanet

Congenital familial protracted diarrhea with enterocyte brush-border abnormalities as a Disease

Congenital familial protracted diarrhea with enterocyte brush-border abnormalities: Another name for Microvillus Inclusion Disease (or close medical condition association).
  »Introduction: Microvillus Inclusion Disease
  »Symptoms of Microvillus Inclusion Disease

Symptoms of Congenital familial protracted diarrhea with enterocyte brush-border abnormalities (Microvillus Inclusion Disease)

Some of the symptoms of Congenital familial protracted diarrhea with enterocyte brush-border abnormalities incude:

• Chronic diarrhea
• Dehydration
• Acidosis
• Retarded growth
• Developmental delay

See full list of 9 symptoms of Congenital familial protracted diarrhea with enterocyte brush-border abnormalities (Microvillus Inclusion Disease)

Congenital familial protracted diarrhea with enterocyte brush-border abnormalities: Related Disease Topics

These medical disease topics may be related to Congenital familial protracted diarrhea with enterocyte brush-border abnormalities:

• Davidson's disease
• congenital microvillous atrophy
• metabolic acidosis
• intestinal transplant

Terms associated with Congenital familial protracted diarrhea with enterocyte brush-border abnormalities:

Terms Similar to Congenital familial protracted diarrhea with enterocyte brush-border abnormalities:

• Davidson disease
• Intractable diarrhea of infancy
• Microvillus atrophy, congenital
• Microvillus inclusion disease

Source - NIH

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