Ahmad M, Abbas H, Haque S, Flatz G
Hum Genet. 1987 Feb;75(2):169-73. doi: 10.1007/BF00591081.
A Pakistani kindred comprising seven generations and 36 members with the split-hand/split-foot anomaly is described. The full expression of the trait, monodactylous or split hand and split foot, mainly of the lobster-claw type, was present in 33 males and 3 females. Other females showed a distinctly milder expression of the trait, usually in the form of partial syndactyly, metacarpal and phalangeal hypoplasia, and malformation. The distribution of the affected members in the pedigree is compatible with X-chromosomal inheritance. Hemizygous males and presumably homozygous females exhibit the typical split-hand/split-foot anomaly, whereas only a part of the obligatory heterozygous females show the milder expression. There were no associated anomalies, such as ectodermal dysplasia, cleft lip/palate, macular degeneration, malformations of the long bones or internal organs, and overt mental retardation.
本文描述了一个包含七代、36名成员的巴基斯坦家族,该家族存在并指/并趾畸形。该性状的完全表现形式,即单指或并指并趾,主要为龙虾爪型,出现在33名男性和3名女性身上。其他女性表现出该性状明显较轻的表达形式,通常为部分并指、掌骨和指骨发育不全以及畸形。家系中受影响成员的分布符合X染色体遗传。半合子男性和推测的纯合子女性表现出典型的并指/并趾畸形,而只有一部分必然的杂合子女性表现出较轻的表达形式。没有相关的异常情况,如外胚层发育不良、唇腭裂、黄斑变性、长骨或内脏畸形以及明显的智力迟钝。