๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Complex I deficiency with diabetes, Fanconi syndrome and mtDNA deletion

โœ Scribed by A. Luder; V. Barash


Book ID
104900271
Publisher
Springer
Year
1994
Tongue
English
Weight
129 KB
Volume
17
Category
Article
ISSN
0141-8955

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Type I diabetes mellitus in a patient wi
โœ Elder, Deborah A. ;Kaiser-Rogers, Kathleen ;Aylsworth, Arthur S. ;Calikoglu, Ali ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 76 KB ๐Ÿ‘ 2 views

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