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41. Links: - Alabama Council For Developmental Disabilities
These are just a few of the topics discussed. Disorders. Aarskog Syndrome;Aase Syndrome; Abetalipoproteinemia; ablepharonmacrostomia syndrome;
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44. WebGuest Directory - Health : Conditions And Diseases : Genetic Disorders
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45. WebGuest Directory - Health : Conditions And Diseases : Rare Disorders
Health Conditions and Diseases Rare Disorders. Aarskog Syndrome;Aase Syndrome; Abetalipoproteinemia; ablepharonmacrostomia syndrome;
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  • Cherubs - A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia. Contact a Family - Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK. Fibrosing Mediastinitis - The least common, but most severe, late complication of histoplasmosis. Educational and research information. Includes interviews, patient stories, and a community forum. Fibrous Dysplasia Support Online - For those seeking support and information concerning the rare bone diseases: fibrous dysplasia, McCune Albright Syndrome and Cherubism. Human Growth Foundation - Information about growth-related disorders through education, research, and advocacy. Member driven organization. International Rare Disease Support Network - A community providing more than a 1000 different links to support groups for the people of all nations.

46. Startplane /Health/Conditions_and_Diseases/Genetic_Disorders/Ablepharon-Macrosto
ablepharonmacrostomia syndrome. See also Links. Ablepharon Macrostomia Syndrome- A personal site with information and links about this disease.
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47. SLCentral Directory - Health - Conditions And Diseases - Rare Disorders
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    50. Health > Conditions And Diseases > Genetic Disorders
    WAGR Syndrome; Wilson s Disease. Aarskog Syndrome; Aase Syndrome;ablepharonmacrostomia syndrome; Alagille Syndrome; Alkaptonuria;Alpha
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    Gene Clinics
    Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients. http://www.geneclinics.org

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    54. Ablepharon Macrostomia Syndrome
    Ablepharon Macrostomia syndrome. This page is dedicated to AblepharonMacrostomia syndrome or AMS. Information on AMS has been provided
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    Ablepharon Macrostomia Syndrome
    This page is dedicated to Ablepharon Macrostomia Syndrome or AMS.
    Information on AMS has been provided by the National Organization for Rare Disorders (NORD) and by personal experience and extensive research.
    Ablepharon Macrostomia Syndrome is an extremely rare inherited genetic disorder that is characterized by different physical abnormalities that affect the head and facial areas, skin, fingers, and the genitalia. The people affected by AMS may also have malformations of the nipples and the abdominal wall.
    Some of the characteristics of AMS are: lack of or under-developed eyelids(Ablepharon), absence of eyelashes and eyebrows, wide fish-like mouths(Macrostomia), and/or incompletely developed, low set ears. Eye abnormalities may occur due to the ablepharon. People with AMS can also have abnormally sparse, thin hair; coarse, dry, thickened skin with excessive folds. They may have webbed fingers with limited extension of the fingers and may have malformations of the external genitalia. In some cases of AMS, the individual has absent or very small nipples and/or protrusion of portions of the large intestine through an opening in the abdominal wall (abdominal or ventral hernia)
    The cause of Ablepharon Macrostomia Syndrome is not known, but some of the cases suggest that AMS may be inherited as an autosomal recessive genetic trait.

    55. Www.angelfire.com/ga2/ams/
    NORD National Organization for Rare Disorders, Inc.Ablepharon Macrostomia syndrome. To purchase full-text report ($7.50) Copyright1997, 2001, 2002 Synonyms of Ablepharon Macrostomia syndrome AMS.
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    56. NORD - National Organization For Rare Disorders, Inc.
    syndrome) AIDS Dysmorphic syndrome APECED syndrome Aarskog syndrome Aase syndromeAblepharon Macrostomia syndrome Acanthocheilonemiasis Acanthocytosis
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    58. ORPHANET - Rare Diseases - Orphan Drugs
    D I S E A S E Ablepharon macrostomia syndrome. ICD Q87.0
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    59. Ablepharon Macrostomia Syndrome
    Ablepharon Macrostomia syndrome Important It is possible that the main title ofthe report Ablepharon Macrostomia syndrome is not the name you expected.
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    You are in Medical Library Choose a Topic Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... For a Complete Report Ablepharon Macrostomia Syndrome Important It is possible that the main title of the report Ablepharon Macrostomia Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms
    • AMS
    Disorder Subdivisions
    • None
    General Discussion Ablepharon-Macrostomia Syndrome (AMS) is an extremely rare inherited disorder characterized by various physical abnormalities affecting the head and facial (craniofacial) area, the skin, the fingers, and the genitals. In addition, affected individuals may have malformations of the nipples and the abdominal wall. Infants and children with AMS may also experience delays in language development and, in some cases, mental retardation. Resources Children's Craniofacial Association 13140 Coit Road Dallas, TX 75240

    60. Index
    Muscle Deficiency syndrome Abdominal Wall Defect Abercrombie syndrome Abiotrophicophthalmoplegia externa Ablepharon Macrostomia syndrome Abnormal Pap Test
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