61. Ablepharon Macrostomia Syndrome Inc. Ablepharon Macrostomia syndrome. Children with AblepharonMacrostomiasyndrome may experience delayed language development. In http://www.bchealthguide.org/kbase/nord/nord1093.htm

document.write(''); var hwPrint=1; var hwDocHWID="nord1093"; var hwDocTitle="Ablepharon Macrostomia Syndrome"; var hwRank="1"; var hwSectionHWID="nord1093"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Ablepharon Macrostomia Syndrome Important It is possible that the main title of the report 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 Related Disorders List Information on the following diseases can be found in the Related Disorders section of this report: Barber-Say Syndrome Associated Congenital Disorders (General) 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. Symptoms Ablepharon-Macrostomia Syndrome (AMS), an extremely rare inherited disorder, is characterized by distinctive malformations affecting the head and facial (craniofacial) area; abnormalities of the skin, the fingers, and/or the genitals; additional physical abnormalities; delayed language development; and/or, in some cases, mental retardation.

62. Health Library - Ablepharon Macrostomia syndrome. Synonyms Disorder Subdivisions GeneralDiscussion Resources National Organization for Rare Disorders. http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw

63. 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://www.meritcare.com/hwdb/showTopic.asp?pd_hwid=nord1093

64. Health: Conditions And Diseases Trachoma, Uveitis. Genetic Disorders Aarskog syndrome, Aase syndrome, AblepharonMacrostomiasyndrome. Alagille syndrome, Alkaptonuria, Alpha-1 Antitrypsin Deficiency. http://www.puredirectory.com/Health/Conditions-and-Diseases/

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65. Health, Conditions And Diseases, Genetic Disorders: Ablepharon-Macrostomia Syndr Ablepharon Macrostomia syndrome is an extremely rare inherited genetic disorder thatis characterized by different physical abnormalities that affect the head http://www.combose.com/Health/Conditions_and_Diseases/Genetic_Disorders/Ablephar

Top Health Conditions and Diseases Genetic Disorders ... Ablepharon-Macrostomia Syndrome Related links of interest: Health:Conditions and Diseases:Rare Disorders Ablepharon Macrostomia Syndrome - A personal site with information and links about this disease. Human Genome Mapping Project - A list of features for Ablepharon-Macrostomia Syndrome. NORD: Ablepharon Macrostomia Syndrome - A look at the alternate name, a general discussion and further resources. OMIM: National Center for Biotechnology Information - A clinical synopsis for Ablepharon-Macrostomia syndrome. 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. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor The combose.com directory is based on the Open Directory and has been modified and enhanced using our own technology. About ComboSE Download Combose Toolbar

66. ORPHANET - Rare Diseases - Orphan Drugs Warning, Site map, Contact, Order the Orphanet book, Printing version, DISEASE Ablepharon macrostomia syndrome, ICD Q87.0, No description is available, MIM 200110, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=920

67. ORPHANET - Rare Diseases - Orphan Drugs The Barber Say syndrome seems to differ from the ablepharon macrostomia syndrome,but it may derive from a different mutation on the same gene. http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1231

68. Health Library - Ablepharon Macrostomia syndrome. Synonyms Disorder Subdivisions GeneralDiscussion Resources National Organization for Rare Disorders. http://12.42.224.152/Library/HealthGuide/IllnessConditions/topic.asp?hwid=nord10

69. Health Library - Ablepharon Macrostomia syndrome. Important It is possible that the main title ofthe report Ablepharon Macrostomia syndrome is not the name you expected. http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

70. Healthwise Topic Ablepharon Macrostomia syndrome, Back to previous page. SynonymsDisorder Subdivisions General Discussion Resources National http://www.stlukes-sf.sutterhealth.org/health/healthinfo/index.cfm?section=healt

71. Healthwise Health Information, Topic Ablepharon Macrostomia syndrome, Back to previouspage. Synonyms Disorder Subdivisions General Discussion Resources http://www.suttercoast.org/health/healthinfo/index.cfm?section=healthinfo&page=a

72. The Medword List - Medical Transcription Directory - The Medword List - Conditio Categories Aarskog syndrome ( 4 ). Aase syndrome ( 1 ). AblepharonMacrostomiasyndrome ( 3 ). Alagille syndrome ( 2 ). Alkaptonuria ( 3 ). http://www.medwordlist.com/Conditions_and_Diseases/Genetic_Disorders/

Top Level Conditions and Diseases : Genetic Disorders Categories: Aarskog Syndrome Aase Syndrome Ablepharon-Macrostomia Syndrome Alagille Syndrome ... Zellweger Syndrome Links: Genetic and Rare Conditions Site popular Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z. http://www.kumc.edu/gec/support/ (Added: Mon Jan 01 2001 Hits: 45 Rating: 0.00 Votes: ) Rate It 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 (Added: Mon Jan 01 2001 Hits: 24 Rating: 0.00 Votes: ) Rate It Primary Ciliary Dyskinesia Information on a rare congenital disease. http://www.p-c-d.org/en/ (Added: Mon Jan 01 2001 Hits: 17 Rating: 0.00 Votes: ) Rate It Spellex medical spell checker is the most up-to-date, and accurate speller ever developed. Perfect for MT work. Medword Store ARISTA 2000 TENS unit provides relief from various types of muscle pain like repetitive stress injury from typing.

73. Mioti: Diseases + Conditions Diseases + Conditions Ablepharon Macrostomia syndrome. Search Mioti http://www.mioti.com/cat/condition/condition.asp?Cat=AblepharonMacro

74. Wauu.DE: Health: Conditions And Diseases: Genetic Disorders: Ablepharon-Macrosto Onlye. Links URL hinzufügen. Ablepharon Macrostomia syndrome Apersonal site with information and links about this disease. http http://www.wauu.de/Health/Conditions_and_Diseases/Genetic_Disorders/Ablepharon-M

Home Health Conditions and Diseases Genetic Disorders : Ablepharon-Macrostomia Syndrome Search DMOZ-Verzeichnis: All Categories Categories Onlye Links: Ablepharon Macrostomia Syndrome A personal site with information and links about this disease. http://www.angelfire.com/ga2/AMS/ Human Genome Mapping Project A list of features for Ablepharon-Macrostomia Syndrome. http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?1084 NORD - Ablepharon Macrostomia Syndrome A look at the alternate name, a general discussion and further resources. OMIM: National Center for Biotechnology Information A clinical synopsis for Ablepharon-Macrostomia syndrome. http://www3.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?200110 © 1998- 2002 Ein Service von Wauu.de UserNet.DE Linktip: MnogoSearch.ORG Map TopTen TopTen eng Aktuelle Linktips Mozilla 1.7 RC 1 Basteln 0190 Warner Free Rund ums Rad ... Fantasy - Shop Webmaster-Links Webspace Free Subdomain Service Merchandise Fun SUMA - Forum ... Abmahnungen œber Wauu Regeln Webmasterservice Impressum b

75. Wauu.DE: Health: Conditions And Diseases: Genetic Disorders Kategorien Aarskog syndrome (6). Aase syndrome (3). AblepharonMacrostomiasyndrome (4). Alagille syndrome (5). Alkaptonuria (4). Alpha http://www.wauu.de/Health/Conditions_and_Diseases/Genetic_Disorders/

Home Health Conditions and Diseases : Genetic Disorders Search DMOZ-Verzeichnis: All Categories Categories Onlye Kategorien: Aarskog Syndrome Aase Syndrome Ablepharon-Macrostomia Syndrome Alagille Syndrome ... Zellweger Syndrome Links: Dr. Greene's HouseCalls A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease. http://www.drgreene.com/html/21614.html 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 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. http://www.kumc.edu/gec/support/ 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. http://www.ctds.info/genetic_disorders.html

76. Birth Disorder Information Directory - A AaAf. Aagenaes syndrome (Cholestasis-Lymphedema syndrome http://www.bdid.com/defectaa.htm

HOME Aa-Af Aagenaes Syndrome (Cholestasis-Lymphedema Syndrome) Cholestasis with lymphedema (Aagenaes syndrome) Aagenaes* Syndrom Aagenaes aagenaes syndrome ... Aagenaes* Syndrom Aarskog (Scott) Syndrome (Faciodigitogenital Syndrome, Faciogenital Dysplasia) List of Sites Aarskog-Like Syndrome (Faciodigitogenital Syndrome, Recessive Form; Teebi Naguib Alawadi Syndrome) Aarskog like syndrome FACIODIGITOGENITAL SYNDROME, RECESSIVE Aarskog Ose Pande Syndrome (Lipodystrophy Rieger Anomaly Diabetes) Aarskog ose pande syndrome LIPODYSTROPHY, PARTIAL, WITH RIEGER ANOMALY, SHORT STATURE, AND INSULINOPENIC DIABETES MELLITUS AASE Syndrome (Anemia with Triphalangeal Thumbs) List of Sites AASE Smith Syndrome (Hydrocephalus with Cleft Palate and Joint Contractures) AASE-Smith - Hydrocephalus; Cleft Palate; Joint Contractures AASE-SMITH SYNDROME AASE Smith Aase-Smith syndrome ABCD Syndrome (Albinism, Black Lock, Cell Migration Disorder of the Neurocytes of the Gut, and Deafness) abcd syndrome ABCD SYNDROME Abdallat Davis Farrage Syndrome (Neurocutaneous Syndrome, Abdallat Type; Spastic Paraplegia-Pigmentary Abnormalities) Abdallat (1980) - Neurocutaneous Syndrome SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES abdallat davis farrage syndrome abdallat davis farrage syndrome Abdominal Muscle Absence/Aplasia/Deficiency/Defect Anomalad/Syndrome See Prune Belly Syndrome Abetalipoproteinemia (Bassen Kornzweig Syndrome) List of Sites Ablepharon -Ichthyosis Syndrome Ablepharon-Ichthyosis -Macrostomia Syndrome Allison has AMS (Has a photo gallery)

77. Birth Disorder Information Directory - BA-BL BaBl. BK Mole syndrome See Melanoma, Familial/Cutaneous Malignant Type. Badersyndrome (Odontomatosis Aortae Oesophagus Stenosis, Odontoma Dysphagia syndrome) http://www.bdid.com/defectba.htm

HOME Ba-Bl B-K Mole Syndrome See Melanoma, Familial/Cutaneous Malignant Type Bader Syndrome (Odontomatosis Aortae Oesophagus Stenosis, Odontoma Dysphagia Syndrome) bader syndrome ODONTOMA-DYSPHAGIA SYNDROME BADS Syndrome See Black Locks with Albinism and Deafness Syndrome Baelz Syndrome (Cheilitis Glandularis) baelz syndrome CHEILITIS GLANDULARIS Bagatelle Cassidy Syndrome (Macrocephaly Short Limbs Deafness) bagatelle cassidy syndrome Bahemuka Brown Syndrome (Spastic Paraplegia Facial Cutaneous Lesions) bahemuka brown syndrome Baker Vinters Syndrome (Hydrocephalus Craniosynostosis Bifid Nose) baker vinters syndrome Ballard Syndrome (Brachydactyly, Combined B and E Types; Pitt Williams Brachydactyly) ballard syndrome BRACHYDACTYLY, COMBINED B AND E TYPES Baller Gerold Syndrome See Craniosynostosis-Radial Aplasia Syndrome Ballinger Wallace Syndrome (Diabetes-Deafness Syndrome, Maternally Transmitted; Diabetes Mellitus, Noninsulin-Dependent/Type II, with Deafness) Ballinger-wallace syndrome DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED Bamboo Hair Syndrome See Netherton Disease Bamforth Syndrome (Hypothyroidism, Athyroidal, with Spiky Hair and Cleft Palate)

78. Genetics And Molecular Biology - While differential diagnosis of this disorder should include ablepharonmacrostomiasyndrome (McCarthy and West, 1977; Hornblass and Reifler, 1985, Cesarino et http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572000000200003&l

79. Diseases Uveitis. Genetic Disorders. Aarskog syndrome. Aase syndrome. AblepharonMacrostomiasyndrome. Alagille syndrome. Alkaptonuria. Alpha-1 Antitrypsin Deficiency. Batten. http://diseases.health.designerz.com/diseases-directory.php

Map.Designerz.com Diseases News Diseases Chat Diseases Site Map ... Mexico Web Intelligence about Diseases Designerz, L.L.C

80. Formudes.de - Das Auf Dem Open Directory Basierendes Translate this page Ablepharon Macrostomia syndrome - A personal site with informationand links about this disease. Human Genome Mapping Project - A http://www.formudes.de/index.php/Health/Conditions_and_Diseases/Genetic_Disorder

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