Brachydactyly short stature hypertension (Bilginturan) syndrome: Report on two families

被引:0
|
作者
Chitayat, D
Grix, A
Balfe, JW
Abramowicz, JS
Garza, J
Fong, CT
Silver, MM
Saller, DN
Bresnick, GH
Giedion, A
Lachman, RS
Rimoin, DL
机构
[1] SO CALIF PERMANENTE MED GRP,SACRAMENTO,CA
[2] UNIV ROCHESTER,STRONG MEM HOSP,ROCHESTER,NY 14642
[3] KINDERSPITAL ZURICH,CH-8032 ZURICH,SWITZERLAND
[4] CEDARS SINAI MED CTR,LOS ANGELES,CA 90048
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1997年 / 73卷 / 03期
关键词
hypertension; short stature; brachydactyly; vasculopathy; intracerebral hemorrhage; autosomal dominant;
D O I
10.1002/(SICI)1096-8628(19971219)73:3<279::AID-AJMG10>3.0.CO;2-G
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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. (C) 1997 Wiley-Liss, Inc.
引用
收藏
页码:279 / 285
页数:7
相关论文
共 50 条
  • [21] Short trunk stature, brachydactyly, and platyspondyly in three sibs:: A new form of brachyolmia or a new skeletal dysplasia?
    Tüysüz, B
    Üngür, S
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 119A (03): : 375 - 380
  • [22] Short stature, hearing loss, retinitis pigmentosa, and distinctive facies syndrome: A case report
    Reeves, Ashley
    Ojha, Kanwal
    Meddaugh, Hannah
    Zambrano, Regina M.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2022, 188 (12) : 3535 - 3539
  • [23] Short stature and hypothyroidism in a child with Nail-Patella Syndrome. A case report
    Goecke, C.
    Mellado, C.
    Garcia, C.
    Garcia, H.
    REVISTA CHILENA DE PEDIATRIA-CHILE, 2018, 89 (01): : 107 - 111
  • [24] Case report: A Chinese boy with facial dysmorphism, immunodeficiency, livedo, and short stature syndrome
    Jiang, Lihong
    Chen, Xin
    Zheng, Jiaqi
    Wang, Meilin
    Bo, Hui
    Liu, Geli
    FRONTIERS IN PEDIATRICS, 2022, 10
  • [25] RAB33B and PCNT variants in two Pakistani families with skeletal dysplasia and short stature
    Noor ul Ain
    Zunaira Fatima
    Sadaf Naz
    Outi Makitie
    BMC Musculoskeletal Disorders, 22
  • [26] Klinefelter syndrome and short stature: an unusual combination
    M. P. Bahíllo-Curieses
    M. Fournier-Carrera
    J. Morán-López
    M. J. Martínez-Sopena
    Endocrine, 2011, 39 : 294 - 295
  • [27] RAB33B and PCNT variants in two Pakistani families with skeletal dysplasia and short stature
    Ain, Noor ul
    Fatima, Zunaira
    Naz, Sadaf
    Makitie, Outi
    BMC MUSCULOSKELETAL DISORDERS, 2021, 22 (01)
  • [28] Identification and functional analysis of NPR2 truncating mutations in two Chinese families with short stature
    Shuoshuo Wei
    Rong Li
    Dongye He
    Chuanpeng Zhang
    Mei Zhang
    Yanying Li
    Shuxiong Chen
    Fupeng Liu
    Bo Ban
    Qianqian Zhao
    BMC Pediatrics, 25 (1)
  • [29] Brachydactyly Type A3 Is More Commonly Seen in Children With Short Stature But Does Not Affect Their Height Improvement by Growth Hormone Therapy
    Wu, Huahong
    Li, Yang
    Li, Hui
    FRONTIERS IN ENDOCRINOLOGY, 2022, 13
  • [30] A novel CEP57 variant associated with mosaic variegated aneuploidy syndrome in a Chinese female presenting with short stature, microcephaly, brachydactyly, and small teeth
    Feng, Biyun
    Chang, Guoying
    Zhang, Qianwen
    Li, Xin
    Tang, Yijun
    Gu, Shili
    Wang, Yirou
    Wang, Jian
    Wang, Xiumin
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2022, 10 (06):