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Indian J Pediatr ; 2002 Jun; 69(6): 531-2
Article Dans Anglais | IMSEAR | ID: sea-79090

Résumé

This syndrome comprises of bilateral femoral hypoplasia and unusual facies comprises of short nose with broad tip, elongated philtrum, thin upper lip, small lower jaw, cleft palate and antimongolian slant of palpebral fissure. Etiology is idiopathic, sporadic, few families have been reported to have autosomal dominant inheritance. We report a case with the additional finding of unilateral complete aplasia of femur, encephalocele, complete cleft lip, bilateral absence of 5th metatarsal and toe and hypospadias. The mode of inheritance appears to be sporadic mutation in this case.


Sujets)
Malformations multiples/anatomopathologie , Bec-de-lièvre/anatomopathologie , Face/malformations , Fémur/malformations , Humains , Hypospadias/anatomopathologie , Nouveau-né , Mâle , Orteils/malformations
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