Björnsson A, Arnason A, Tippet P
Department of Plastic Surgery, Landspitalinn University Hospital, Reykjavík, Iceland.
Cleft Palate J. 1989 Jan;26(1):3-8.
Information was available on 293 family members and spouses of seven generations in an Icelandic family with high frequency of cleft of secondary palate and ankyloglossia. The authors have personally investigated 182 individuals in generations IV-VII and have drawn blood from over 100 members for genetic marker studies. The senior author, Dr. Björnsson, has operated on two-thirds of the affected individuals. Twenty-six family members had cleft palate (CP) and, of these, 19 (17 male and two females) had ankyloglossia as well (CP + A). Twenty females and one male had only ankyloglossia (A). All mothers in one of two branches of the family who had sons with CP + A had ankyloglossia themselves. This was not the case in the other branch, in which the mothers of affected sons were themselves unaffected. Fathers affected with CP, CP + A, or high vaulted palate (HVP) never had affected sons. As reported earlier, the condition has been mapped to the q13-q21 region of the X chromosome using restriction fragment length polymorphism (RFLP) techniques (Moore et al, 1987). Our conclusion is that this midline defect is X-linked but varies in the severity of expression.
在一个冰岛家族中,有293名七代以内的家庭成员及配偶的相关信息,该家族中腭裂和舌系带过短的发生率很高。作者亲自调查了IV - VII代中的182名个体,并从100多名成员身上采集了血液用于基因标记研究。资深作者比约恩松医生为三分之二的患病个体实施了手术。26名家庭成员患有腭裂(CP),其中19名(17名男性和2名女性)同时患有舌系带过短(CP + A)。20名女性和1名男性仅患有舌系带过短(A)。在家族两个分支之一中,所有生育了患有CP + A儿子的母亲自身都患有舌系带过短。另一个分支的情况并非如此,该分支中患病儿子的母亲自身并未患病。患有CP、CP + A或高拱腭(HVP)的父亲从未有过患病的儿子。如先前报道,利用限制性片段长度多态性(RFLP)技术已将该病定位到X染色体的q13 - q21区域(Moore等人,1987年)。我们的结论是,这种中线缺陷是X连锁的,但表达严重程度有所不同。