Congenital duplication of the palm in a patient with multiple anomalies

被引：16
|
作者：
Al-Qattan, MM [1 ]
机构：
[1] King Saud Univ, Div Plast Surg, Riyadh, Saudi Arabia
来源：
JOURNAL OF HAND SURGERY-BRITISH AND EUROPEAN VOLUME | 2003年 / 28B卷 / 03期
关键词：
D O I：
10.1016/S0266-7681(02)00084-0
中图分类号：
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学（修复外科学）];
学科分类号：
摘要：
In 1995, Parr and McMahon described a syndrome of congenital duplication of footpads in mice which lacked a protein called,'Wingless-type mouse mammary tumour virus integration site family member 7a' (Wnt-7a). This syndrome has not been described in humans and the following report describes a similar syndrome in a Saudi girl. The role of Wnt-7a in the development of the limb along the dorso-ventral axis is discussed, along with interaction between the Wnt-7a and other axes of limb growth.
引用
收藏
页码：276 / 279
页数：4
相关论文
共 50 条
  • [1] Incomplete bladder duplication with multiple congenital anomalies: A rare presentation
    Awasthi, Nipun Kumar
    Goel, Hemantkumar
    Mahapatra, Rajkumarsingha
    Pal, Dilipkumar
    UROLOGY ANNALS, 2015, 7 (01) : 88 - 90
  • [2] Clinical and molecular delineation of 16p13.3 duplication in a patient with congenital heart defect and multiple congenital anomalies
    Chen, Jin-Lan
    Yang, Yi-Feng
    Huang, Can
    Wang, Jian
    Yang, Jin-Fu
    Tan, Zhi-Ping
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (03) : 685 - 688
  • [3] Congenital duplication of the palm syndrome
    Al-Qattan, M. M.
    Eyaid, Waaa
    Al-Balwi, Mohammed
    ANNALS OF PLASTIC SURGERY, 2007, 59 (03) : 341 - 343
  • [4] Inherited 18q23 duplication in a fetus with multiple congenital anomalies
    Isidor, Bertrand
    Winer, Norbert
    Joubert, Madeleine
    Boisseau, Pierre
    Le Caignec, Cedric
    Boceno, Michelle
    Fallet, Catherine
    David, Albert
    Rival, Jean Marie
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2008, 51 (03) : 231 - 238
  • [5] DUPLICATION OF THE VHL AND IRAK2 GENES IN A PATIENT WITH MENTAL RETARDATION/MULTIPLE CONGENITAL ANOMALIES, EPILEPSY AND ECTOMORPHIC HABITUS
    Chabchoub, E.
    Michils, G.
    Vermeesch, J. R.
    De Cock, P.
    Lagae, L.
    Fryns, J. P.
    GENETIC COUNSELING, 2010, 21 (01): : 35 - 40
  • [6] Duplication 1q32-q44 and multiple congenital anomalies.
    Bayani, J
    Xu, J
    Freeman, V
    Watts, J
    Smith, PA
    Squire, J
    Nowaczyk, MJM
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A157 - A157
  • [7] Congenital absence of the portal vein in a patient with multiple vascular anomalies
    Ogul, Hayri
    Bayraktutan, Ummugulsum
    Yalcin, Ahmet
    Turan, Mehmet Ibrahim
    Ozgokce, Mesut
    Eren, Suat
    Kantarci, Mecit
    SURGICAL AND RADIOLOGIC ANATOMY, 2013, 35 (06) : 529 - 534
  • [8] Idiopathic retrograde duodenojejunal intussusception in a patient with multiple congenital anomalies
    Lobo, Liana Mae Jajurie
    Lopez, Marc Paul Jose
    Deogracias, Jan Miguel
    Lim, Michael Geoffrey Lee
    BMJ CASE REPORTS, 2025, 18 (02)
  • [9] Concurrence of multiple types of eyelid synkinesia in a patient with congenital anomalies
    Ishiyama, Akihiko
    Saito, Yoshiaki
    Sugai, Kenji
    Sasaki, Masayuki
    Yamazaki, Hiroko
    Kohama, Masanori
    BRAIN & DEVELOPMENT, 2012, 34 (02) : 140 - 142
  • [10] Triple mosaic variants of PURA in a patient with multiple congenital anomalies
    Fujita, Atsushi
    Suenaga, Yuta
    Takeshita, Eri
    Takahashi, Yuji
    Suzuki, Yuichi
    Ohori, Sachiko
    Tsuchida, Naomi
    Uchiyama, Yuri
    Koshimizu, Eriko
    Miyatake, Satoko
    Mizuguchi, Takeshi
    Matsumoto, Naomichi
    JOURNAL OF HUMAN GENETICS, 2025, 70 (04) : 227 - 230
12345