Background - Cases of diabetes mellitus associated with Turner syndrom
e are noninsulin-dependent. We report a case of insulin-dependent diab
etes mellitus (IDDM) with Turner syndrome. Case report. - An 11 year-o
ld girl with Turner syndrome was investigated for glucose tolerance th
at was normal with glycosylated hemoglobin at 5.1%. The patient was th
en given growth hormone plus oxandrolone until the age of 15 yr 3 mo;
estrogen replacement was initiated at 15 yr 9 mo and progesterone 6 mo
nths later. At the age of 16.5 yrs, the patient developed manifestatio
ns of diabetes mellitus with polyuria, polydipsia, weight loss. Blood
glucose concentration was 415 mg/dl with ketoacidosis. She was given i
nsulin; at that time, blood insulin level was 7 mU/ml, C-peptide 0.8 n
g/ml and glycosylated hemoglobin Alc 8.2%. Islet cell auto-antibodies
were positive (1/80) and histocompatibility antigens were A1, A2, B14,
B18, CW7, DR7, DR11, DQ7. After 6 months treatment ment, blood insuli
n and C-peptide after IV glucagon were nil. There was no familial case
of IDDM. Conclusions. - This ease of IDDM seems to be the first repor
ted in Turner syndrome. This IDDM could be a manifestation of autoimmu
nity.