Saadi Abdelkrim, Borck Guntram, Boddaert Nathalie, Chekkour Mohamed Chahine, Imessaoudene Belaïd, Munnich Arnold, Colleaux Laurence, Chaouch Malika
Department of Neurology, Etablissement hospitalier spécialisé de Benaknoun, and Department of Biochemistry, Centre Hospitalo-Universitaire Mustapha Bacha, Algiers, Algeria.
Eur J Med Genet. 2009 Jul-Aug;52(4):180-4. doi: 10.1016/j.ejmg.2009.03.013. Epub 2009 Mar 28.
Homozygous mutations in the ASPM gene are a major cause of autosomal recessive primary microcephaly (MCPH). Here we report on a consanguineous Algerian family in which three out of five children presented with severe microcephaly, simplified cortical gyration, mild to severe mental retardation and low to low-normal birth weight. Given the parental consanguinity with the unaffected parents being third cousins once removed, the most probable pattern of inheritance was autosomal recessive. Linkage and mutational analyses identified compound heterozygous truncating mutations within the ASPM gene segregating with MCPH (c.2389C>T [p.Arg797X] and c.7781_7782delAG [p.Gln2594fsX6]). These results highlight some of the pitfalls of genetic analysis in consanguineous families. They also suggest that low birth weight may be a feature of MCPH, a finding that needs confirmation, and confirm that ASPM mutations are associated with simplified cortical gyration.
ASPM基因的纯合突变是常染色体隐性原发性小头畸形(MCPH)的主要病因。在此,我们报告一个近亲结婚的阿尔及利亚家庭,该家庭的五个孩子中有三个患有严重小头畸形、脑回简化、轻至重度智力发育迟缓以及低至正常低限的出生体重。鉴于父母为近亲结婚,未受影响的父母是隔了一代的第三代堂亲,最可能的遗传模式为常染色体隐性遗传。连锁分析和突变分析确定了ASPM基因内的复合杂合截短突变与MCPH共分离(c.2389C>T [p.Arg797X]和c.7781_7782delAG [p.Gln2594fsX6])。这些结果凸显了近亲家庭遗传分析中的一些陷阱。它们还表明低出生体重可能是MCPH的一个特征,这一发现有待证实,并证实ASPM突变与脑回简化有关。