Clinical and radiological assessment of a family with mild brachydactyly type A1: the usefulness of metacarpophalangeal profiles

被引:16
作者
Armour, CM
Bulman, DE
Hunter, AGW
机构
[1] Childrens Hosp Eastern Ontario, Dept Genet, Ottawa, ON K1K 1N2, Canada
[2] Ottawa Gen Hosp, Inst Res, Ottawa, ON K1H 8L6, Canada
[3] Ottawa Gen Hosp, Div Neurol, Ottawa, ON K1H 8L6, Canada
关键词
brachydactyly A1; metacarpophalangeal profile;
D O I
10.1136/jmg.37.4.292
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The brachydactylies are a group of conditions in which various subtypes have been defined based upon the specific pattern of digital bones involved. Type Al brachydactyly is principally characterised by maximal involvement of the middle phalanges. We report an extended family with a mild brachydactyly Al which was, except for some short stature, not associated with any of the additional clinical findings reported in several published families. While all the hand bones tended to be small, the principal features of the affected members were shortened middle and distal phalanges, proximal Ist phalanges, and 5th metacarpals. The feet were similarly involved and tended to have a broad, slightly adducted forefoot. The two affected children showed multiple coned epiphyses. This paper provides a detailed description of the family including the radiographic signs and metacarpophalangeal profiles, which proved to be useful in distinguishing the mildly affected persons.
引用
收藏
页码:292 / 296
页数:5
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