Hay-Wells syndrome: A case report

被引：1
|
作者：
Khalfi, L. [1 ]
Hamama, J. [1 ]
Mahroug, L. [1 ]
Arrob, A. [1 ]
Sabani, H. [1 ]
El Khatib, K. [1 ]
机构：
[1] Hop Mil Instruct Mohammed V, Serv Stomatol & Chirurg Maxillofaciale, Rabat 10100, Morocco
来源：
ARCHIVES DE PEDIATRIE | 2016年 / 23卷 / 02期
关键词：
CLEFT-LIP; P63; PALATE;
D O I：
10.1016/j.arcped.2015.11.016
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
Hay-Wells syndrome is a rare form of ectodermal dysplasia. We report a case of a 5-year-old girl, the daughter of non-consanguineous parents. She had the characteristic of facial dysmorphia of Hay-Wells syndrome. Molecular analysis confirmed diagnosis. The patient had a cleft palate, which is considered one of cardinal signs of this syndrome. She underwent Veau-Wardill-Kilner palatoplasty with satisfactory results. Through this case report, we describe the maxillofacial manifestations of this syndrome with a literature review. (C) 2015 Elsevier Masson SAS. All rights reserved:
引用
收藏
页码：163 / 166
页数：4
相关论文
共 50 条
  • [1] Hay-Wells syndrome - A case report
    de Freitas Rosa, Dario Junior
    Machado, Ronaldo Figueiredo
    Martins Neto, Marcelino Pereira
    Montenegro de Sa, Alessandra Almeida
    Gamonal, Aloisio
    ANAIS BRASILEIROS DE DERMATOLOGIA, 2010, 85 (02) : 232 - 235
  • [2] Hay-Wells syndrome (AEC): a case report
    Macias, Emilio
    de Carlos, Felix
    Cobo, Juan
    ORAL DISEASES, 2006, 12 (05) : 506 - 508
  • [3] HAY-WELLS SYNDROME - REPORT OF THE 1ST ITALIAN CASE
    CLEMENTI, M
    BELLATO, S
    TUROLLA, L
    ORZALI, A
    TENCONI, R
    RIVISTA ITALIANA DI PEDIATRIA-ITALIAN JOURNAL OF PEDIATRICS, 1991, 17 (03): : 327 - 329
  • [4] Hay-wells syndrome of ectodermal dysplasia
    Kulkarni M.L.
    Deshmukh S.
    Matani D.
    Gayatri K.
    The Indian Journal of Pediatrics, 2006, 73 (1) : 101 - 101
  • [5] Head and neck manifestations of Hay-Wells syndrome
    Propst, EJ
    Campisi, P
    Papsin, BC
    OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2005, 132 (01) : 165 - 166
  • [6] Hay-wells syndrome with selective immunoglobulin a deficiency
    Sharanya, Bhupathi
    Narayanan, Rajendran
    Karunanandhan, Manobalan
    INDIAN JOURNAL OF PAEDIATRIC DERMATOLOGY, 2020, 21 (04) : 307 - 309
  • [7] Expanding the genetic profile of Hay-Wells syndrome
    Romero-Perez, D.
    Encabo-Duran, B.
    Ramon-Sapena, R.
    ACTAS DERMO-SIFILIOGRAFICAS, 2018, 109 (06): : 560 - 562
  • [8] A neonate with denuded skin: Hay-Wells syndrome
    Lodha, A
    Ng, E
    CANADIAN MEDICAL ASSOCIATION JOURNAL, 2004, 171 (02) : 131 - 131
  • [9] Hay-Wells syndrome: the challenges of a nine-year follow-up
    de Amorim, Rebecca Perez
    Nakata, Maria Vitoria Yuka Messias
    Gonc, Vitoria Gabrielle De Paula
    Castro, Ivanka Miranda de
    Haddad, Gabriela Roncada
    Abbade, Luciana Patricia Fernandes
    ANAIS BRASILEIROS DE DERMATOLOGIA, 2024, 99 (06)
  • [10] Rapp-Hodgkin ectodermal dysplasia syndrome: The clinical and molecular overlap with Hay-Wells syndrome
    Kannu, P
    Savarirayan, R
    Ozoemena, L
    White, SM
    McGrath, JA
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (08) : 887 - 891
12345