Robinow syndrome.
Article
Dans Anglais
| IMSEAR
| ID: sea-92355
ABSTRACT
Robinow syndrome is a rare congenital abnormality. It is characterized by mesomelic brachymelia, hemivertebrae, dysmorphic facies, genital hypoplasia, micropenis, clinodactyly, camptodactly, hypoplastic nails and moderate short stature. We are documenting the case on the account of its rarity and additional features.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Pénis
/
Achondroplasie
/
Syndrome
/
Malformations multiples
/
Humains
/
Mâle
/
Diagnostic différentiel
/
Nanisme
/
Ectromélie
/
Nourrisson
Type d'étude:
Etude diagnostique
langue:
Anglais
Année:
2000
Type:
Article
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