Rabson-Mendenhall syndrome.
Indian J Med Sci
;
2005 Feb; 59(2): 70-3
Article
Dans Anglais
| 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.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Syndrome
/
Malformations multiples
/
Femelle
/
Humains
/
Insulinorésistance
/
Acidocétose diabétique
/
Odontodysplasie
/
Consanguinité
/
Diabète
/
Retard de croissance staturo-pondérale
langue:
Anglais
Texte intégral:
Indian J Med Sci
Année:
2005
Type:
Article
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