Links: - Alabama Council For Developmental Disabilities These are just a few of the topics discussed. Disorders. Aarskog Syndrome;Aase Syndrome; Abetalipoproteinemia; ablepharonmacrostomia syndrome; http://www.acdd.org/Links/conditions/Rare_Disorders.htm
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PhatNav Directory - Health/Conditions_and_Diseases/A Health/Conditions and Diseases/Genetic Disorders/ablepharonmacrostomia syndrome.Health/Conditions and Diseases/Genetic Disorders/Aarskog Syndrome. http://www.phatnav.com/directory/Health/Conditions_and_Diseases/A.cat
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Extractions: Blepharophimosis Ptosis Epicanthus Inversus Syndrome - The BPEI (BPES) Family Network encourages people to get in touch with each other, share information and ask questions. Explanation of this rare eye disorder. Dr. Greene's HouseCalls - A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease. 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. Genetic Disorders: The Links to Diet - Explores the role of diet in birth defects and genetic disorders. Includes nutritional links to disorders such as Down syndrome, cerebral palsy, homocystinuria, and cystic fibrosis. Genetic and Rare Conditions Site - Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z.
Extractions: 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.
Extractions: Submit a Site SLCentral Directory - Health - Conditions and Diseases - Rare Disorders See also: This category in other languages: French Italian Japanese National Organization for Rare Disorders, Inc. - Information about NORD, its programs, special events and the variety of services offered. Includes a rare disease, organization and orphan drug database. Diseases are listed alphabetically for easy searching.
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A In Health > Conditions And Diseases Abetalipoproteinemia@ (3); ablepharonmacrostomia syndrome@ (4); AbnormalUterine Bleeding@ (6); Achilles Tendonitis@ (9); Achondroplasia http://ilectric.com/glance/Health/Conditions_and_Diseases/A/
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Ablepharon Macrostomia Syndrome Ablepharon Macrostomia syndrome. This page is dedicated to AblepharonMacrostomia syndrome or AMS. Information on AMS has been provided http://www.angelfire.com/ga2/AMS/
Extractions: 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)
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. http://www.angelfire.com/ga2/ams/
NORD - National Organization For Rare Disorders, Inc. syndrome) AIDS Dysmorphic syndrome APECED syndrome Aarskog syndrome Aase syndromeAblepharon Macrostomia syndrome Acanthocheilonemiasis Acanthocytosis http://www.rarediseases.org/search/rdblist.html
ORPHANET - Rare Diseases - Orphan Drugs D I S E A S E Ablepharon macrostomia syndrome. ICD Q87.0 http://orphanet.infobiogen.fr/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=920
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. http://my.webmd.com/hw/health_guide_atoz/nord1093.asp
Extractions: 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.
Index Muscle Deficiency syndrome Abdominal Wall Defect Abercrombie syndrome Abiotrophicophthalmoplegia externa Ablepharon Macrostomia syndrome Abnormal Pap Test http://my.webmd.com/hw/index/index-topics-A.asp
