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Symptomatic anal anomalies in chromosome 22q11 deletion syndrome: a report of three patients

โœ Scribed by Mudaffer Al-Mudaffer; Prem Puri; William Reardon


Book ID
106056553
Publisher
Springer-Verlag
Year
2006
Tongue
English
Weight
152 KB
Volume
22
Category
Article
ISSN
0179-0358

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We describe a patient with type I diabetes, clinical ยฎndings consistent with velocardiofacial syndrome, and a chromosome 22q11.2 deletion. A nine-year-old boy presented with a history of polyuria, polydipsia, weight loss, hyperglycemia, ketosis, serum insulin antibodies, and a low C-peptide level. H