Spektrum złożonego niedoboru odporności i enteropatii

Kod Orpha: 436252Kod OMIM: 243150

Definicja

A rare genetic disease characterized by multiple intestinal atresia in association with combined immunodeficiency and inflammatory bowel disease. Clinical features include widespread atresia extending from the stomach to the rectum, homogenous calcifications in the abdominal cavity, hepatic cholestasis, cirrhosis, and chronic liver failure, hypoplastic thymus, and increased susceptibility to mainly bacteria and viruses. The immunological phenotype consists of profound generalized T-cell lymphopenia and milder natural killer cell and B-cell lymphopenia, as well as low serum levels of IgG, IgA, and IgM, with elevated serum IgE. The disease is mostly fatal in infancy or childhood.

Dane
Klasyfikacja

Choroba

Synonimy
CID-MIA/early-onset IBD
CID-MIA/IBD o wczesnym początku
Kod ORPHA
436252
Kod OMIM
243150
Kod ICD10
Q82.8
Kod ICD11
-

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