WAARDENBURG SYNDROME TYPE 1 AND A RARE FINDING OF ANAL ATRESIA

被引:0
|
作者
Tasdemir, S. [1 ]
Erdem, H. B. [1 ]
Sahin, I. [1 ]
Kara, M. [2 ]
Tatar, A. [1 ]
机构
[1] Ataturk Univ, Fac Med, Dept Med Genet, TR-25240 Erzurum, Turkey
[2] Ataturk Univ, Fac Med, Dept Pediat, TR-25240 Erzurum, Turkey
来源
GENETIC COUNSELING | 2015年 / 26卷 / 04期
关键词
PAIRED DOMAIN;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
引用
收藏
页码:467 / 470
页数:4
相关论文
共 50 条
  • [21] Waardenburg-Shah syndrome (WS type IV): a rare case from Pakistan
    Taimoor Ashraf Khan
    C. Aqeel Safdar
    Shehryar Zameer
    Arshad Khushdil
    Perioperative Medicine, 9
  • [22] Waardenburg-Shah syndrome (WS type IV): a rare case from Pakistan
    Khan, Taimoor Ashraf
    Safdar, C. Aqeel
    Zameer, Shehryar
    Khushdil, Arshad
    PERIOPERATIVE MEDICINE, 2020, 9 (01)
  • [23] 2 RARE COMPLICATIONS IN OPERATED RECTAL AND ANAL ATRESIA
    VONBODMANN, J
    HECKER, WC
    ZEITSCHRIFT FUR KINDERCHIRURGIE-SURGERY IN INFANCY AND CHILDHOOD, 1988, 43 (01): : 56 - 58
  • [24] Rhizomelia with anal atresia and anophthalmia:: a new syndrome?
    Oezlem, Giray
    Elcin, Bora
    Ayfer, Ulgenalp
    Oguz, Ates
    Erdener, Oezer
    Derya, Ercal
    CLINICAL DYSMORPHOLOGY, 2008, 17 (01) : 53 - 56
  • [25] Multiple hyperpigmented patches in Waardenburg syndrome type 1: An unusual presentation
    Morgaonkar, Manjaree
    Gupta, Savera
    Vyas, Kapil
    Jain, Suresh Kumar
    INDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY, 2016, 82 (06): : 711 - U254
  • [26] Rare Association of Waardenburg Syndrome with Minimal Change Disease
    Anvesh, G.
    Raju, S. B.
    Prasad, K.
    Sharma, A.
    Surendra, M.
    INDIAN JOURNAL OF NEPHROLOGY, 2018, 28 (03) : 226 - 228
  • [27] Clinical and genetic study of Waardenburg syndrome type 1 in Tunisian patients
    Skouri, Sana
    Achour, Ahlem
    Nouira, Malek
    Maazoul, Faouzi
    Benoit, Valerie
    Ghazi, Besbes
    M'rad, Ridha
    Trabelsi, Mediha
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 112 - 113
  • [28] Development of a molecular genetic diagnostic service for Waardenburg syndrome Type 1 and Type 3
    McKay, Fiona
    Jenkins, L.
    Glindzicz, M. Bitner
    Lench, N.
    JOURNAL OF MEDICAL GENETICS, 2010, 47 : S63 - S63
  • [29] Waardenburg Syndrome: A Rare Disorder with an Uncommon Manifestation in a Neonate
    Khushdil, Arshad
    Anees, Umair
    Hussain, Moeez
    JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN, 2024, 34 (09): : 1139 - 1140
  • [30] MOLECULAR ABNORMALITIES OF TYPE-1 AND TYPE-2 OF WAARDENBURG-SYNDROME
    DREYFUS, JC
    M S-MEDECINE SCIENCES, 1995, 11 (01): : 133 - 133