Fraser syndrome in three consecutive siblings

Fraser syndrome (FS) is a rare disorder characterized by a combination of acrofacial and urogenital malformations with or without cryptophthalmos. We report a newborn and its two elder siblings who had multiple congenital anomalies and clinico-radiological features consistent with FS.

Detalles Bibliográficos
Autores principales: Kalaniti, Kaarthigeyan, Sandhya, V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160077/
https://www.ncbi.nlm.nih.gov/pubmed/21897626
http://dx.doi.org/10.4103/0974-620X.83661

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160077/
https://www.ncbi.nlm.nih.gov/pubmed/21897626
http://dx.doi.org/10.4103/0974-620X.83661

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