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.
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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