Roberts-SC Phocomelia Syndrome: Case Report
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Case Report
P: 66-68
June 2012

Roberts-SC Phocomelia Syndrome: Case Report

Med Bull Haseki 2012;50(2):66-68
1. Erzurum Nenehatun Kadın Doğum Hastanesi, Genetik Ünitesi, Erzurum, Türkiye
2. Erzurum Nenehatun Kadın Doğum Hastanesi, Yenidoğan Ünitesi, Erzurum, Türkiye
No information available.
No information available
Received Date: 14.12.2011
Accepted Date: 27.01.2012
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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.