Rabson-Mendenhall syndrome: a case report
IJCN-Iranian Journal of Child Neurology. 2010; 4 (1): 49-52
Dans Anglais
| IMEMR
| ID: emr-123718
ABSTRACT
Rabson-Mendenhall syndrome is a rare genetic disorder characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, dysplastic dentition, coarse facial features, paradoxical fasting hypoglycemia, postprandial hyperglycemia, extreme hyperinsulinemia and pineal hyperplasia. Herein, we described a 10-year-old girl with physical features of the Rabson-Mendenhall syndrome that was presented with polyuria. To our knowledge, this is the first report of the Rabson-Mendenhall syndrome from Iran
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Indice:
Méditerranée orientale
Sujet Principal:
Polyurie
/
Insulinorésistance
/
Clitoris
/
Diabète
/
Hirsutisme
Type d'étude:
Enquête cas-témoins / Études cas/témoins
Limites du sujet:
Femelle
/
Humains
langue:
Anglais
Texte intégral:
Iran. J. Child Neurol.
Année:
2010
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