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RobertsSC Fokomeli Sendromu: Olgu Sunumu
2012
Journal:  
Haseki Tıp Bülteni
Author:  
Abstract:

Roberts-SC phocomelia syndrome is an autosomal recessive inherited malformation characterized by symmetric limb defects, craniofacial abnormalities, prenatal and postnatal growth retardation and mental retardation. A premature baby born at 34 weeks gestation was admitted to Erzurum Nenehatun Obstetrics and Gynecology Hospital Neonate Unit due to congenital anomaly, growth retardation, cleft palate, hypoplasia of the nose, low-set ears, and bilateral shortness of the forearms. Here, we present a rare case of Roberts-SC phocomelia syndrome.

Keywords:

RobertsSC Focomeli Syndrome: Case Presentation
2012
Author:  
Abstract:

Roberts-SC phocomelia syndrome is an autosomal recessive inherited malformation characterized by symmetric limb defects, craniofacial abnormalities, prenatal and postnatal growth retardation and mental retardation. A premature baby born at 34 weeks gestation was admitted to the Neonate Unit due to congenital anomaly, growth retardation, cleft palate, hypoplasia of the nose, low-set ears, and bilateral shortness of the forearms. Here, we present a rare case of Roberts-SC phocomelia syndrome.

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Haseki Tıp Bülteni

Field :   Sağlık Bilimleri

Journal Type :   Uluslararası

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Article : 847
Cite : 379
Haseki Tıp Bülteni