医学
Diamond–Blackfan贫血
特雷彻-柯林斯综合征
闭锁
贫血
解剖
传导性听力损失
中耳
内科学
遗传学
颅面
核糖体
核糖核酸
精神科
基因
生物
作者
Alicia McFarren,Somasundaram Jayabose,M. Fevzi Özkaynak,Oya Tugal,Claudio Sandoval
标识
DOI:10.1097/mph.0b013e31805d8f45
摘要
Diamond-Blackfan anemia (DBA) is associated with congenital anomalies especially of the midline. When present, facial anomalies are reminiscent of Treacher-Collins syndrome, and both DBA and Treacher-Collins syndrome are disorders of ribosomal biogenesis. Herein, we describe a female infant with multiple midline defects associated with DBA and reaffirm the absence of RPS-19 mutations in DBA patients with facial anomalies.
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