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Indian J Med Sci ; 2005 Feb; 59(2): 70-3
Article in English | IMSEAR | ID: sea-66043

ABSTRACT

Rabson-Mendenhall syndrome is characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, premature and dysplastic dentition, coarse facial features, paradoxical fasting hypoglycemia and post-prandial hyperglycemia, extreme hyperinsulinemia and pineal hyperplasia. We describe a six-month-old female child with physical features suggestive of the Rabson-Mendenhall syndrome. The child also had medullary nephrocalcinosis.


Subject(s)
Abnormalities, Multiple/genetics , Acanthosis Nigricans/genetics , Consanguinity , Diabetes Mellitus/blood , Diabetic Ketoacidosis/genetics , Failure to Thrive , Female , Growth Disorders/genetics , Hirsutism/genetics , Humans , Infant , Insulin Resistance/genetics , Odontodysplasia/genetics , Syndrome
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