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Cornelia de lange syndrome.
Indian J Hum Genet ; 2008 Jan; 14(1): 23-26
Artículo en Inglés | IMSEAR | ID: sea-138846
ABSTRACT

BACKGROUND:

Cornelia de Lange syndrome (CDLS) is a rare multiple congenital anomaly syndrome characterized by a distinctive facial appearance, developmental delay, growth retardation, low birth weight, skeletal formation anomaly, and hirsutism. CASE Here for the first time a case of CDLS from Iran, a 15-week-old male infant who was refereed as a case of multiple congenital anomalies. Clinical investigation showed that the child was a case of CDLS.

CONCLUSION:

This is the first case report with CDLS in Iran.

Texto completo: Disponible Índice: IMSEAR (Asia Sudoriental) Idioma: Inglés Revista: Indian J Hum Genet Año: 2008 Tipo del documento: Artículo

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Texto completo: Disponible Índice: IMSEAR (Asia Sudoriental) Idioma: Inglés Revista: Indian J Hum Genet Año: 2008 Tipo del documento: Artículo