Diseases & Conditions


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Ectrodactyly Ectodermal Dysplasia Cleft Lip/Palate


Synonyms of Ectrodactyly Ectodermal Dysplasia Cleft Lip/Palate
  • Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome
  • EEC Syndrome

Disorder Subdivisions



    General Discussion
    Ectrodactyly-Ectodermal Dysplasia-Cleft Lip/Palate (EEC Syndrome) is a rare form of ectodermal dysplasia inherited as an autosomal dominant genetic trait the symptoms of which can vary from mild to severe. The most common symptoms found in patients with EEC Syndrome are: missing or irregular fingers and/or toes (ectrodactyly), abnormalities of the hair and glands, cleft lip and/or palate, or unusual facial features, as well as abnormalities of the eyes and urinary tract.

    Organizations related to Ectrodactyly Ectodermal Dysplasia Cleft Lip/Palate
    • Ectodermal Dysplasia Society
      108 Charlton Lane
      Glos. None GL53 9EA
      Phone #: +44- 12-42 261332
      800 #: N/A
      e-mail: diana@ectodermaldysplasia.org
      Home page: http://www.ectodermaldysplasia.org
    • MUMS (Mothers United for Moral Support, Inc) National Parent-to-Parent Network
      150 Custer Court
      Green Bay WI 54301-1243
      Phone #: 920-336-5333
      800 #: 877-336-5333
      e-mail: mums@netnet.net
      Home page: http://www.netnet.net/mums/
    • NIH/National Arthritis and Musculoskeletal and Skin Diseases Information Clearinghouse
      1 AMS Circle
      Bethesda MD 20892-3675
      Phone #: 301-495-4484
      800 #: 877-226-4267
      e-mail: NIAMSinfo@mail.nih.gov
      Home page: http://www.niams.nih.gov/Health_Info
    • National Foundation for Ectodermal Dysplasias
      410 East Main Street
      Mascoutah IL 62258-0114
      Phone #: 618-566-2020
      800 #: --
      e-mail: info@nfed.org
      Home page: http://www.nfed.org



    For a Complete Report

    This is an abstract of a report from the National Organization for Rare Disorders, Inc. ? (NORD). A copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html