Ectrodactyly-ectodermal dysplasia-clefting syndrome causing blindness in a child

被引:4
|
作者
Rosenberg, Jamie B. [1 ]
Butrus, Salim [2 ]
Bazemore, Marlet G. [3 ]
机构
[1] Montefiore Med Ctr, Dept Ophthalmol, Bronx, NY 10467 USA
[2] George Washington Univ Hosp, Georgetown Univ Hosp, Washington, DC USA
[3] Childrens Natl Med Ctr, Washington, DC 20010 USA
来源
JOURNAL OF AAPOS | 2011年 / 15卷 / 01期
关键词
LIP-PALATE SYNDROME; OCULAR MANIFESTATIONS; EEC-SYNDROME; DRY EYE; EVAPORATION;
D O I
10.1016/j.jaapos.2010.12.001
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Ectrodactyly-ectodermal dysplasia-clefting syndrome, the result of a mutation in the gene encoding tumor protein p63, causes ocular surface disease. It is typically progressive, with vision loss in adulthood. We present a case of severe corneal disease, glaucoma, and blindness related to ectrodactyly-ectodermal dysplasia-clefting syndrome in a 3-year-old female patient.
引用
收藏
页码:80 / 82
页数:3
相关论文
共 50 条
  • [31] KERATOPATHY IN A FAMILY WITH THE ECTRODACTYLY ECTODERMAL DYSPLASIA-CLEFTING SYNDROME
    MAWHORTER, LG
    RUTTUM, MS
    KOENIG, SB
    OPHTHALMOLOGY, 1985, 92 (10) : 1427 - 1431
  • [32] Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome Associated With p63 Mutation and an Uncommon Phenotype
    Ribeiro Paranaiba, Livia Mans
    Martelli- Junior, Hercilio
    de Miranda, Roseli Teixeira
    Bufalino, Andreia
    Abdo Filho, Ruy Camargo
    Coletta, Ricardo D.
    CLEFT PALATE-CRANIOFACIAL JOURNAL, 2010, 47 (05): : 544 - 547
  • [33] NORMAL IMMUNOLOGICAL STATUS IN 4 PATIENTS WITH ECTRODACTYLY-ECTODERMAL DYSPLASIA-CLEFTING SYNDROME (EEC-SYNDROME)
    OBEL, N
    HANSEN, B
    BLACK, FT
    CLINICAL GENETICS, 1993, 43 (03) : 146 - 149
  • [34] ECTRODACTYLY-ECTODERMAL DYSPLASIA CLEFTING SYNDROME WITH SCALP DERMATITIS - REPLY
    FOSKO, SW
    STENN, KS
    BOLOGNIA, JL
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1993, 29 (03) : 506 - 506
  • [35] Midface growth in patients with ectrodactyly ectodermal dysplasia-clefting syndrome
    Birgfeld, Craig B.
    Glick, Patricia
    Singh, Davinder
    LaRossa, Don
    Bartlett, Scott
    PLASTIC AND RECONSTRUCTIVE SURGERY, 2007, 120 (01) : 144 - 150
  • [36] Bilateral congenital lacrimal fistulas in an adult as part of ectrodactyly-ectodermal dysplasia-clefting syndrome: A rare anomaly
    Ghosh, Debangshu
    Saha, Somnath
    Basu, Sumit Kumar
    INDIAN JOURNAL OF OPHTHALMOLOGY, 2015, 63 (10) : 800 - 803
  • [37] A sporadic case of oligosymptomatic ectrodactyly-ectodermal dysplasia-clefting syndrome (vol 78, pg 521, 2012)
    Baroni, A.
    Piccolo, V
    Di Maio, R.
    Russo, T.
    INDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY, 2012, 78 (06):
  • [38] PRUNE BELLY ANOMALY ON PRENATAL ULTRASOUND AS A PRESENTING FEATURE OF ECTRODACTYLY-ECTODERMAL DYSPLASIA-CLEFTING SYNDROME (EEC)
    Janssens, S.
    Defoort, P.
    Vandenbroecke, C.
    Scheffer, H.
    Mortier, G.
    GENETIC COUNSELING, 2008, 19 (04): : 433 - 437
  • [39] Mutations in p63 gene in ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome and their relevance to the ocular phenotype
    Willoughby, CE
    Chen, I
    Ellis, I
    McGrath, JA
    Kaye, S
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2005, 46
  • [40] GROWTH-HORMONE DEFICIENCY ASSOCIATED WITH THE ECTRODACTYLY-ECTODERMAL DYSPLASIA-CLEFTING SYNDROME AND ISOLATED ABSENT SEPTUM PELLUCIDUM
    KNUDTZON, J
    AARSKOG, D
    PEDIATRICS, 1987, 79 (03) : 410 - 412