Chitayat D, Grix A, Balfe J W, Abramowicz J S, Garza J, Fong C T, Silver M M, Saller D N, Bresnick G H, Giedion A, Lachman R S, Rimoin D L
Hospital for Sick Children, Toronto, Ontario, Canada.
Am J Med Genet. 1997 Dec 19;73(3):279-85. doi: 10.1002/(sici)1096-8628(19971219)73:3<279::aid-ajmg10>3.0.co;2-g.
We report on two families with autosomal dominant brachydactyly of hands and feet and hypertension. All affected members of the first family had proportionate short stature. However, the propositus and the affected relatives in the second family were only short compared to unaffected relatives. The hypertension was medically responsive in all cases. The propositus in the second family had poor compliance and a striking generalized vasculopathy. All patients were of normal intelligence and had a normal facial appearance. The brachydactyly-short stature-hypertension syndrome was first reported by Bilginturan et al. [1973] in a Turkish family and the families reported by us are Caucasian and Hispanic. The gene causing this condition in the original Turkish family was recently mapped to 12p. Our report expands our existing knowledge and the ethnic diversity of this syndrome.
我们报告了两个患有常染色体显性遗传的手足短指症和高血压的家族。第一个家族的所有患病成员均身材比例矮小。然而,第二个家族的先证者及患病亲属仅相较于未患病亲属身材矮小。在所有病例中,高血压对药物治疗有反应。第二个家族的先证者依从性差且患有明显的全身性血管病变。所有患者智力正常,面部外观正常。短指症 - 身材矮小 - 高血压综合征最早由比尔金图兰等人[1973年]在一个土耳其家族中报道,而我们报告的家族是白种人和西班牙裔。导致最初土耳其家族出现这种病症的基因最近被定位到12号染色体短臂。我们的报告扩展了我们对该综合征的现有认知以及其种族多样性。