Merlob P, Steier D, Reisner S H
Neonatology Department, Beilinson Medical Centre, Petah Tiqva, Israel.
J Med Genet. 1988 Nov;25(11):750-3. doi: 10.1136/jmg.25.11.750.
A large family (13 affected members in three generations) is reported in which isolated microcephaly occurred without any other dysmorphic or neurological abnormalities. The family pedigree confirms the autosomal dominant mode of inheritance with incomplete penetrance, including one example of male to male transmission and the occurrence of a non-manifesting heterozygote resulting in a 'skipped generation'. There is considerable variation in the phenotypic expression of autosomal dominant microcephaly. This isolated (uncomplicated) type of microcephaly should be distinguished from other well defined, dominantly inherited forms of microcephaly.
据报道,有一个大家庭(三代中有13名受影响成员),其中出现了孤立性小头畸形,且无任何其他畸形或神经异常。家系图谱证实了常染色体显性遗传模式且具有不完全外显率,包括一例男性对男性的传递以及一个未表现出症状的杂合子导致“隔代遗传”的情况。常染色体显性小头畸形的表型表达存在相当大的差异。这种孤立性(无并发症)小头畸形类型应与其他明确的、显性遗传的小头畸形形式区分开来。