Bowcock A M, van Tonder S, Jenkins T
Br J Haematol. 1984 Jan;56(1):69-78. doi: 10.1111/j.1365-2141.1984.tb01272.x.
The child with haemoglobin H (HbH) disease and multiple congenital abnormalities reported by Borochowitz et al (1970) has been more fully investigated in view of the recent report by Weatherall et al (1981) of a 'new' syndrome of HbH disease and mental retardation. Restriction enzyme analysis indicates that the child's HbH disease results from the inheritance of an alpha-thalassaemia 2 chromosome (-alpha/) from his mother and, from his father, a chromosome which has undergone a deletion including the zeta- and alpha-globin genes as well as an undefined length of DNA. Striking similarities between our patient and Weatherall et al's patients at the clinical level and between our patient and their patient number 1 at the molecular level, confirm that a new syndrome has been defined.
鉴于韦瑟罗尔等人(1981年)报告了一种“新的”血红蛋白H(HbH)病与智力发育迟缓综合征,博罗乔维茨等人(1970年)报告的患有HbH病和多种先天性异常的儿童已得到更全面的研究。限制性内切酶分析表明,该儿童的HbH病是由于从母亲那里遗传了一条α地中海贫血2染色体(-α/),并从父亲那里遗传了一条发生缺失的染色体,该缺失包括ζ和α珠蛋白基因以及一段长度未明的DNA。我们的患者与韦瑟罗尔等人的患者在临床水平上以及我们的患者与他们的1号患者在分子水平上的显著相似性,证实了一种新综合征已被确定。