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伴有非缺失型α地中海贫血的X连锁智力迟钝(ATR-X):对表型的进一步描述。

X linked mental retardation with non-deletional alpha thalassaemia (ATR-X): further delineation of the phenotype.

作者信息

Ogle R, DeSouza M, Cunningham C, Kerr B, Sillence D

机构信息

Department of Genetics, Children's Hospital, Camperdown, Australia.

出版信息

J Med Genet. 1994 Mar;31(3):245-7. doi: 10.1136/jmg.31.3.245.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6155/1049752/5cfdd8afa1d5/jmedgene00282-0073-a.jpg

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