| Literature DB >> 9632175 |
I Kaitila1, E Savilahti, T Ormälä.
Abstract
The clinical phenotype of Schimke immunoosseous dysplasia (SID) is characterized by growth retardation, renal failure, recurrent infections, cerebral infarcts, and skin pigmentation beginning in childhood. We report here on a 4-year-old male child who had all characteristic symptoms of SID, and, in addition, vomiting and prolonged diarrhea. The study results suggest that malabsorption, demonstrated as increased serum immunoglobulin A anti-gliadin antibody, steatorrhea and partial villous atrophy of the jejunal small bowel, is a previously unrecognized feature of SID.Entities:
Mesh:
Year: 1998 PMID: 9632175
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299