Waardenburg syndrome type I with heterochromia iridis and circumscribed hypo pigmentation of the skin

被引:0
|
作者
Eigelshoven, S. [1 ]
Kameda, G. [2 ]
Kortuem, A. [1 ]
Huebsch, S. [3 ]
Angerstein, W. [4 ]
Singh, P. [5 ]
Voehringer, R.
Goecke, T. [6 ]
Mayatepek, E. [2 ]
Ruzicka, T. [1 ,7 ]
Wildhardt, G. [8 ]
Meissner, T. [2 ]
Kruse, R. [1 ]
机构
[1] Univ Dusseldorf, Dept Dermatol, D-40225 Dusseldorf, Germany
[2] Univ Dusseldorf, Dept Gen Pediat, D-40225 Dusseldorf, Germany
[3] Univ Dusseldorf, Dept Ophthalmol, D-40225 Dusseldorf, Germany
[4] Univ Dusseldorf, Dept Pedaudiol, D-40225 Dusseldorf, Germany
[5] Univ Dusseldorf, Dept Dent & Endodont, D-40225 Dusseldorf, Germany
[6] Univ Dusseldorf, Inst Human Genet, D-40225 Dusseldorf, Germany
[7] Univ Munich, Dept Dermatol, D-8000 Munich, Germany
[8] Ctr Human Genet, Ingelheim, Germany
关键词
D O I
暂无
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
引用
收藏
页码:176 / 176
页数:1
相关论文
共 50 条
  • [1] WAARDENBURG SYNDROME TYPE I WITH HETEROCHROMIA IRIDIS AND CIRCUMSCRIBED HYPOPIGMENTATION OF THE SKIN
    Eigelshoven, Sibylle
    Kameda, Gitta
    Kortuem, Anne-Katrin
    Huebsch, Simone
    Angerstein, Wolfgang
    Singh, Preeti
    Voehringer, Renate
    Goecke, Timm
    Mayatepek, Ertan
    Ruzicka, Thomas
    Wildhardt, Gabriele
    Meissner, Thomas
    Kruse, Roland
    PEDIATRIC DERMATOLOGY, 2009, 26 (06) : 759 - 761
  • [2] A PEDIGREE OF BINOCULAR HETEROCHROMIA IRIDIS ASSOCIATED WITH OTHER ANOMALIES (WAARDENBURG-KLEIN SYNDROME)
    BASILE, R
    JOURNAL DE GENETIQUE HUMAINE, 1965, 14 (2-3): : 87 - +
  • [3] Waardenburg Syndrome Type I
    Gowda, Vykuntaraju K.
    Srinivas, Sahana
    Srinivasan, Varunvenkat M.
    INDIAN JOURNAL OF PEDIATRICS, 2020, 87 (03): : 244 - 244
  • [4] Waardenburg Syndrome Type I
    Vykuntaraju K. Gowda
    Sahana Srinivas
    Varunvenkat M. Srinivasan
    The Indian Journal of Pediatrics, 2020, 87 : 244 - 244
  • [5] A SIBLING PAIR WITH IRIS HETEROCHROMIA, DEAFNESS, AND ATAXIA - A NEW-TYPE OF WAARDENBURG SYNDROME (WS)
    BIRD, LM
    JONES, MC
    PEDIATRIC RESEARCH, 1995, 37 (04) : A82 - A82
  • [6] Waardenburg syndrome type I: case report
    Vieira da Silva, Patricia Capua
    Rangel, Paula
    Couto, Abelardo, Jr.
    ARQUIVOS BRASILEIROS DE OFTALMOLOGIA, 2011, 74 (03) : 209 - 210
  • [7] Waardenburg Syndrome Type I in an Iranian Female
    Tayebi, Naeimeh
    IRANIAN JOURNAL OF PEDIATRICS, 2009, 19 (02) : 189 - 192
  • [8] Otopathology in a case of type I Waardenburg's syndrome
    Merchant, SN
    McKenna, MJ
    Baldwin, CT
    Milunsky, A
    Nadol, JB
    ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 2001, 110 (09): : 875 - 882
  • [9] LOCALIZATION OF A GENE FOR WAARDENBURG SYNDROME TYPE-I
    READ, AP
    FOY, C
    NEWTON, V
    HARRIS, R
    ANNALS OF THE NEW YORK ACADEMY OF SCIENCES-SERIES, 1991, 630 : 143 - 151
  • [10] LOCALIZATION OF A GENE FOR WAARDENBURG SYNDROME TYPE-I
    READ, AP
    FOY, C
    NEWTON, VE
    AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 6 - 6