Genotype-phenotype correlation in hereditary multiple exostoses

被引:139
作者
Francannet, C
Cohen-Tanugi, A
Le Merrer, M
Munnich, A
Bonaventure, J
Legeai-Mallet, L
机构
[1] INSERM, U393, Unite Rech Handicaps Genet & Enfant, F-75743 Paris 15, France
[2] Hop Hotel Dieu, Serv Pediat & Genet B, Clermont Ferrand, France
关键词
hereditary multiple exostoses; EXT1; EXT2; chondrosarcoma;
D O I
10.1136/jmg.38.7.430
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Hereditary multiple exostoses (HME) is a genetically heterogeneous autosomal dominant disorder characterised by the development of bony protuberances mainly located on the long bones. Three HME loci have been mapped to chromosomes 8q24 (EXT1), 11p11-13 (EXT2), and 19p (EXT3). The EXT1 and EXT2 genes encode glycosyltransferases involved in biosynthesis of heparan sulphate proteoglycans. Here we report on a clinical survey and mutation analysis of 42 HME French families and show that EXT1 and EXT2 accounted for more than 90% of HME cases in our series. Among them, 27/42 cases were accounted for by EXT1 (64%, four nonsense, 19 frameshift, three missense, and one splice site mutations) and 9/42 cases were accounted for by EXT2 (21%, four nonsense, two frameshift, two missense, and one splice site mutation). Overall, 31/36 mutations were expected to cause loss of protein function (86%). The most severe forms of the disease and malignant transformation of exostoses to chondrosarcomas were associated with EXT1 mutations. These findings provide the first genotype-phenotype correlation in HME and will, it is hoped, facilitate the clinical management of these patients.
引用
收藏
页码:430 / 434
页数:5
相关论文
共 50 条
  • [21] Hereditary multiple exostoses: are there new plausible treatment strategies?
    Pacifici, Maurizio
    EXPERT OPINION ON ORPHAN DRUGS, 2018, 6 (06): : 385 - 391
  • [22] Developmental pattern of the hip in patients with hereditary multiple exostoses
    Ya-Zhou Wang
    Kwang-Won Park
    Chang-Seon Oh
    Yeong-Seub Ahn
    Qing-Lin Kang
    Sung-Taek Jung
    Hae-Ryong Song
    BMC Musculoskeletal Disorders, 16
  • [23] Developmental pattern of the hip in patients with hereditary multiple exostoses
    Wang, Ya-Zhou
    Park, Kwang-Won
    Oh, Chang-Seon
    Ahn, Yeong-Seub
    Kang, Qing-Lin
    Jung, Sung-Taek
    Song, Hae-Ryong
    BMC MUSCULOSKELETAL DISORDERS, 2015, 16
  • [24] Sport and physical activity in patients with hereditary multiple exostoses
    D'Ambrosi, Riccardo
    Caldarini, Camilla
    Massari, Giulia
    Facchini, Renato Mario
    Ragone, Vincenza
    CLINICAL CASES IN MINERAL AND BONE METABOLISM, 2018, 15 (03) : 321 - 326
  • [25] Axillary artery pseudoaneurysm secondary to hereditary multiple exostoses
    Atalar, Mehmet
    PEDIATRIC RADIOLOGY, 2025, 55 (01) : 207 - 207
  • [26] Two Siblings Followed Up for Hereditary Multiple Exostoses
    Erol, Meltem
    Yigit, Ozgul
    Adanir, Oktay
    Toksoz, Mehmet
    Narin, Halis
    Gok, Veysel
    Borakay, Dilek
    Konya, Murat
    HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI, 2014, 52 (02): : 116 - 119
  • [27] Bilateral ischiofemoral impingement in a patient with hereditary multiple exostoses
    Viala, Pierre
    Vanel, Daniel
    Larbi, Ahmed
    Cyteval, Catherine
    Laredo, Jean-Denis
    SKELETAL RADIOLOGY, 2012, 41 (12) : 1637 - 1640
  • [28] Tc-99m MDP imaging in hereditary multiple tip exostoses
    Restrepo, JM
    Caride, VJ
    CLINICAL NUCLEAR MEDICINE, 2003, 28 (07) : 589 - 590
  • [29] Popliteal artery pseudo-aneurysm and hereditary multiple exostoses
    Chamlou, R
    Stefanidis, C
    Lambert, T
    Munck, D
    ACTA CHIRURGICA BELGICA, 2002, 102 (06) : 467 - 469
  • [30] Costal chondrosarcoma in a woman with hereditary multiple exostoses - a case report
    Yang, Ze
    Wang, Kaiqiang
    Pu, Jiangtao
    FRONTIERS IN ONCOLOGY, 2025, 15