Caldwell B D
Department of Podiatric Medicine, Ohio College of Podiatric Medicine, Cleveland 44106, USA.
J Am Podiatr Med Assoc. 1996 Jun;86(6):244-8. doi: 10.7547/87507315-86-6-244.
Split hand and split foot is an autosomal dominant disorder that displays several genetic phenomena. These include variable expressivity, reduced penetrance, and segregation distortion. Although not fully understood at the molecular level, all are important in determining transmission of the gene thought to be mapped to the long arm of chromosome 7 (7q21.3-q22.1). These phenomena, therefore, have significant implications for inheritance of split hand and split foot and for proper referral for genetic counseling.
裂手裂足是一种常染色体显性疾病,呈现出多种遗传现象。这些现象包括可变表达、降低的外显率和分离畸变。尽管在分子水平上尚未完全了解,但所有这些现象在确定被认为定位于7号染色体长臂(7q21.3 - q22.1)上的基因的传递方面都很重要。因此,这些现象对于裂手裂足的遗传以及正确转诊进行遗传咨询具有重要意义。