Ablepharon Macrostomia Syndrome Inc. Ablepharon Macrostomia syndrome. Children with AblepharonMacrostomiasyndrome may experience delayed language development. In http://www.bchealthguide.org/kbase/nord/nord1093.htm
Extractions: 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. Information on the following diseases can be found in the Related Disorders section of this report: 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. 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.
Health Library - Ablepharon Macrostomia syndrome. Synonyms Disorder Subdivisions GeneralDiscussion Resources National Organization for Rare Disorders. http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw
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
Extractions: Related links of interest: 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
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
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
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
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=
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
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
Extractions: HOME Aagenaes Syndrome (Cholestasis-Lymphedema Syndrome) Aarskog (Scott) Syndrome (Faciodigitogenital Syndrome, Faciogenital Dysplasia) Aarskog-Like Syndrome (Faciodigitogenital Syndrome, Recessive Form; Teebi Naguib Alawadi Syndrome) Aarskog Ose Pande Syndrome (Lipodystrophy Rieger Anomaly Diabetes) AASE Syndrome (Anemia with Triphalangeal Thumbs) AASE Smith Syndrome (Hydrocephalus with Cleft Palate and Joint Contractures) ABCD Syndrome (Albinism, Black Lock, Cell Migration Disorder of the Neurocytes of the Gut, and Deafness) Abdallat Davis Farrage Syndrome (Neurocutaneous Syndrome, Abdallat Type; Spastic Paraplegia-Pigmentary Abnormalities) Abdominal Muscle Absence/Aplasia/Deficiency/Defect Anomalad/Syndrome Abetalipoproteinemia (Bassen Kornzweig Syndrome) Ablepharon -Macrostomia Syndrome Allison has AMS (Has a photo gallery)
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
Extractions: HOME B-K Mole Syndrome Bader Syndrome (Odontomatosis Aortae Oesophagus Stenosis, Odontoma Dysphagia Syndrome) BADS Syndrome Baelz Syndrome (Cheilitis Glandularis) Bagatelle Cassidy Syndrome (Macrocephaly Short Limbs Deafness) Bahemuka Brown Syndrome (Spastic Paraplegia Facial Cutaneous Lesions) Baker Vinters Syndrome (Hydrocephalus Craniosynostosis Bifid Nose) Ballard Syndrome (Brachydactyly, Combined B and E Types; Pitt Williams Brachydactyly) Baller Gerold Syndrome Ballinger Wallace Syndrome (Diabetes-Deafness Syndrome, Maternally Transmitted; Diabetes Mellitus, Noninsulin-Dependent/Type II, with Deafness) Bamboo Hair Syndrome Bamforth Syndrome (Hypothyroidism, Athyroidal, with Spiky Hair and Cleft Palate)
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
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
