Apert's syndrome.
Indian J Dermatol Venereol Leprol
;
2004 Mar-Apr; 70(2): 105-7
Article
in English
| IMSEAR
| ID: sea-52839
ABSTRACT
Apert's syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynostosis, mid-facial malformations and symmetrical syndactyly. We present a 2-month-old girl having features of Apert's syndrome, with cerebral cortical atrophy and bifurcation of the right first metatarsal base, a hitherto undescribed finding.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Language:
English
Journal:
Indian J Dermatol Venereol Leprol
Year:
2004
Type:
Article
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