Ogle R, DeSouza M, Cunningham C, Kerr B, Sillence D
Department of Genetics, Children's Hospital, Camperdown, Australia.
J Med Genet. 1994 Mar;31(3):245-7. doi: 10.1136/jmg.31.3.245.
Two sibs with non-deletional alpha thalassaemia and mental retardation (ATR-X) have been ascertained showing variable neurological features. The proband had a complex neurological picture with recurrent apnoea, complex partial seizures, and prolonged periods of semiconsciousness between 12 and 17 months of age. Episodes of spontaneous laughter were also a feature. An EEG was initially normal. Hb H inclusions were present but rare in this family. The sole genital anomaly was deficiency of the foreskin, a feature not previously described in ATR-X.
已确诊两名患有非缺失型α地中海贫血和智力发育迟缓(ATR-X)的同胞兄妹,他们表现出不同的神经学特征。先证者有复杂的神经学表现,在12至17个月大时出现反复呼吸暂停、复杂部分性癫痫发作以及长时间的半昏迷状态。自发性大笑发作也是一个特征。脑电图最初正常。该家族中存在Hb H包涵体,但很少见。唯一的生殖器异常是包皮缺失,这是ATR-X中以前未描述过的特征。