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Rabson-Mendenhall syndrome.
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.
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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Syndrome / Abnormalities, Multiple / Female / Humans / Insulin Resistance / Diabetic Ketoacidosis / Odontodysplasia / Consanguinity / Diabetes Mellitus / Failure to Thrive Language: English Journal: Indian J Med Sci Year: 2005 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Syndrome / Abnormalities, Multiple / Female / Humans / Insulin Resistance / Diabetic Ketoacidosis / Odontodysplasia / Consanguinity / Diabetes Mellitus / Failure to Thrive Language: English Journal: Indian J Med Sci Year: 2005 Type: Article