Rabson-Mendenhall syndrome: a case report
IJCN-Iranian Journal of Child Neurology. 2010; 4 (1): 49-52
Dans En
| IMEMR
| ID: emr-123718
Responsable en Bibliothèque :
EMRO
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:
IMEMR
Sujet Principal:
Polyurie
/
Insulinorésistance
/
Clitoris
/
Diabète
/
Hirsutisme
Type d'étude:
Case_reports
Limites du sujet:
Female
/
Humans
langue:
En
Texte intégral:
Iran. J. Child Neurol.
Année:
2010