41. DermIS / Main Menu / DOIA / Ectodermal Dysplasia / Info information on the diagnosis ectodermal dysplasia . definition. DEFECTO ECTODERMICO CONGENITO, DISPLASIA ECTODERMICA. Do YOU suffer from ectodermal dysplasia ? http://dermis.multimedica.de/doia/diagnose.asp?zugr=d&lang=e&diagnr=757360&topic

42. DermIS / Main Menu / DOIA / Hidrotic Ectodermal Dysplasia / Info // information on the diagnosis Hidrotic ectodermal dysplasia . synonyms. Clouston Syndrome. definition. Do YOU suffer from Hidrotic ectodermal dysplasia ? http://dermis.multimedica.de/doia/diagnose.asp?zugr=d&lang=e&diagnr=9435&topic=i

43. Anhidrotic Ectodermal Dysplasia Information Diseases Database Anhidrotic ectodermal dysplasia,ChristSiemens-Touraine syndrome,Hypohidrotic X-linked ectodermal dysplasia, Disease Database Information. http://www.diseasesdatabase.com/ddb29810.htm

Diseases Database Index Sponsors Contact ... Previous Page Anhidrotic ectodermal dysplasia Information Search 3 synonyms or equivalents were found. Anhidrotic ectodermal dysplasia aka/or Christ-Siemens-Touraine syndrome aka/or Hypohidrotic X-linked ectodermal dysplasia may cause or feature (Follow link for list) belong(s) to the category of (Follow link for list) No UMLS definitions Anhidrotic ectodermal dysplasia: specific sites Send Anhidrotic ectodermal dysplasia to medical search engines (JavaScript enabled browsers only) If your browser has no JavaScript you can still use these: Search using Internet medical databases Search using Internet search engines (non-specialist) We subscribe to the HONcode principles of the Health On the Net Foundation i-medicine.info - the evidence based medicine, informatics and audit portal Valid XHTML 1.0 Served 2004-06-02 12:03:04 Metadata Updated 2004-05-22

44. Hidrotic Ectodermal Dysplasia Information Diseases Database Hidrotic ectodermal dysplasia aka/or Clouston syndrome No UMLS definitions. Medical information linksHidrotic ectodermal dysplasia specific sites. http://www.diseasesdatabase.com/ddb32043.htm

Diseases Database Index Sponsors Contact ... Previous Page Hidrotic ectodermal dysplasia Information Search 2 synonyms or equivalents were found. Hidrotic ectodermal dysplasia aka/or Clouston syndrome may cause or feature (Follow link for list) belong(s) to the category of (Follow link for list) No UMLS definitions Hidrotic ectodermal dysplasia: specific sites Send Hidrotic ectodermal dysplasia to medical search engines (JavaScript enabled browsers only) If your browser has no JavaScript you can still use these: Search using Internet medical databases Search using Internet search engines (non-specialist) We subscribe to the HONcode principles of the Health On the Net Foundation i-medicine.info - the evidence based medicine, informatics and audit portal Valid XHTML 1.0 Served 2004-06-02 12:03:04 Metadata Updated 2004-05-22

45. Welcome To The UC Davis Children's Hospital Cleft & Craniofacial Program ectodermal dysplasia (EDS) is a term including several conditions. All these way. There are over 150 types of ectodermal dysplasia. There http://www.ucdmc.ucdavis.edu/cleft/craniofacial/guide/about/ectodermaldysplasia.

Home Craniofacial Anomalies About Craniofacial Anomalies Team Approach to Care ... Scheduling an Appointment Ectodermal dysplasia (EDS) is a term including several conditions. All these conditions show differences in the formaiton of parts of the body derived from the ectoderm. The ectoderm is one of three tissue layers found in very early embryonic development. It is involved in the formation of several parts of the body including the skin, hair, nails, teeth, mucous membranes, parts of the inner ear and the lens and retina of the eye. Dysplasia is a term which means something did not develop the way it should have. For a condition to be called ectodermal dysplasia at least two parts of the body derived from the embryonic ectoderm need to have not developed in the normal way. There are over 150 types of ectodermal dysplasia. There are several different ways that ectodermal dysplasia can be inherited, X-linked autosomal dominant and autosomal recessive . The inheritance pattern followed and the parts of the ectoderm affected will depend on which type of ectodermal dysplasia is involved. What are the features of Ectodermal Dysplasia?

46. Ectodermal Dysplasia - Medical Dictionary Definitions Of Popular Medical Terms MedicineNet Home MedTerms medical dictionary AZ List ectodermal dysplasia. Advanced Search. There are a number of different types of ectodermal dysplasia. http://www.medterms.com/script/main/art.asp?articlekey=20848

47. Disease Directory : Genetic Disorders : Ectodermal Dysplasia Diseases Genetic Disorders ectodermal dysplasia. AllRefer Health ectodermal dysplasia Prevention (Anhidrotic ectodermal dysplasia. http://www.diseasedirectory.net/Genetic_Disorders/Ectodermal_Dysplasia/default.a

Wednesday, June 02, 2004 Genetic Disorders Aarskog Syndrome Aase Syndrome Ablepharon-Macrostomia Syndrome ... Genetic Disorders : Ectodermal Dysplasia AllRefer Health - Ectodermal Dysplasia Prevention (Anhidrotic ... - Ectodermal Dysplasia (Anhidrotic Ectodermal Dysplasia) information center covers Prevention. Ectodermal Dysplasia. Ectodermal Dysplasia. Anhydrotic Ectodermal Dysplasia - HUM-MOLGEN - student at Emory University School of Medicine, and I was wondering if anyone knows of a laboratory that test a potential carrier of Ectodermal Dysplasia. Ectodermal Dysplasia - Library E - F. Ectodermal Dysplasia. Ectodermal Dysplasia Support for people and families affected by the various forms of ectodermal dysplasia. Ectodermal Dysplasia - More about Ectodermal Dysplasia. CAUSE OF ECTODERMAL DYSPLASIA: Ectodermal Dysplasia is caused by a single abnormal gene or pair of abnormal genes. Ectodermal Dysplasia - Ectodermal Dysplasia - Patient UK. A directory of UK health, disease, illness Ectodermal Dysplasia. UK sources of information and / or support Ectodermal Dysplasia - Ectodermal Dysplasia. Hypohidrotic: See Ectodermal Dysplasia, Anhidrotic/Hypohidrotic. Margarita Island Type/Type IV: ECTODERMAL DYSPLASIA, TYPE 4; ED4.

48. BASAN ECTODERMAL DYSPLASIA Features Listed For ECTRODACTYLYectodermal dysplasia-CLEFTING (EEC). McKusick 129900. Absent/hypoplastic thymus; Blepharophimosis http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?520

49. BASAN ECTODERMAL DYSPLASIA Features Listed For BASAN ectodermal dysplasia. McKusick 129200. Conjunctivitis; Fused labia; Hypohidrotic or dry skin; Joint laxity; http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?162

50. Www.icondata.com/health/pedbase/files/HIDROTIC.HTM Hypohidrotic ectodermal dysplasiaHypohidrotic ectodermal dysplasia (HED) is a rare inherited multisystem disorder that belongs to the group of diseases known as ectodermal dysplasias. http://www.icondata.com/health/pedbase/files/HIDROTIC.HTM

51. Ectrodactyly Ectodermal Dysplasia Cleft Lip/Palate Ectrodactylyectodermal dysplasia-Cleft Lip/Palate (EEC Syndrome) is a rare form of ectodermal dysplasia inherited as an autosomal dominant genetic trait the http://www.bchealthguide.org/kbase/nord/nord935.htm

document.write(''); var hwPrint=1; var hwDocHWID="nord935"; var hwDocTitle="Ectrodactyly Ectodermal Dysplasia Cleft Lip/Palate"; var hwRank="1"; var hwSectionHWID="nord935"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Ectrodactyly Ectodermal Dysplasia Cleft Lip/Palate 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 Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome EEC Syndrome Disorder Subdivisions None Related Disorders List Information on the following diseases can be found in the Related Disorders section of this report: Ectodermal Dysplasias Rapp-Hodgkins Syndrome Growth Hormone Deficiency 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. Symptoms The most common symptoms of Ectrodactyly-Ectodermal Dysplasia-Cleft Lip/Palate are: absent or irregular fingers and/or toes (ectrodactyly); and/or abnormalities of the eyes, glands, skin, teeth and urinary tract. Any combination of the following symptoms may be present in affected patients.

52. Genetic Disorders, Ectodermal Dysplasia Submit Your Site to the ectodermal dysplasia category. Sponsored ectodermal dysplasia Sites. Submit Your Site to the ectodermal dysplasia category. http://www.iseekhealth.com/ectodermal_dysplasia-1581.php

Home About Us Contact Submit Your Site Search : Home Health Conditions and Diseases Genetic Disorders ... Ectodermal Dysplasia More Ectodermal Dysplasia Categories: Submit Your Site to the Ectodermal Dysplasia category Sponsored Ectodermal Dysplasia Sites Cystic Fibrosis Book Store At WellnessBooks.com Comprehensive source to books on Cystic Fibrosis. Includes community boards and chat, book reviews and online ordering. Buy Genetic Disorders Products We link to merchants which offer Genetic Disorders products for sale. Online Doctors - Ask Us Now! Kasamba's variety of health experts- including Doctors, Specialists, Herbalists, Nurses and more- offer real help for affordable consultation fees- live via chat or e-mail! Buy Genetics Books At Amazon.com and Save! Would you like to save on Genetics Books at Amazon and other stores? Compare prices at BookSellersNow.com! Our site continually proves that online shopping can be fun! Ectodermal Dysplasia Society - Information about the organization as well as the ED condition. Includes links, news articles and contact details. National Foundation for Ectodermal Dysplasia - ED organization based in North America offering information/advice to individuals and supporting scientific research. Includes a newsletter, publications, FAQs and a list of services.

53. Health Library - ectodermal dysplasias. Synonyms. None. Disorder Subdivisions. RappHodgkin Hypohidrotic ectodermal dysplasias; Nail Dystrophy-Deafness Syndrome; http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw

54. Ectodermal Dysplasia, Hypohidrotic The Sleep Tight Video© Help for sleepless parents, Encyclopedia Index E ectodermal dysplasia, hypohidrotic, Search. ectodermal dysplasia, hypohidrotic. http://www.drhull.com/EncyMaster/E/ectodermal_dysplasia.html

Help for sleepless parents Encyclopedia Index E ectodermal dysplasia, hypohidrotic Search ectodermal dysplasia, hypohidrotic Hypohidrotic (anhidrotic) ectodermal dysplasia is a rare, genetically determined condition consisting of three elements: partial or complete absence of sweat glands, abnormal teeth, and sparse hair. Because it is inherited as an X-linked recessive trait, it generally affects only males, but girls who are carriers may also show some signs of the syndrome to greater or lesser degrees. Affected children are unable to sweat. This means that they may experience sometimes mysterious episodes of high fever in warm environments, which makes the condition one to be considered during investigation of a case of fever of unknown origin. Hidrotic ectodermal dysplasia (Clouston syndrome) is a variant condition, characterized by malformed or absent nails, sparse hair, and thickened palms and soles. It is an autosomal dominant hereditary disorder. The teeth are usually normal, although some children have small teeth with weak enamel and numerous caries. Inflammation of the eyes and lids are common. Sweating is always normal. Some patients exhibit absence of eyebrows and lashes, and dark pigmentation over the knees, elbows, and knuckles.

55. Hypohidrotic Ectodermal Dysplasia - The Knowledge Database Of The Swedish Nation Hypohidrotic ectodermal dysplasia. To the Swedish version ectodermal dysplasia Anhidrotic ectodermal dysplasia EDA I ChristSiemens-Touraine Syndrome. http://www.sos.se/smkh/2002-110-10/2002-110-10.htm

Socialstyrelsen 106 30 Stockholm e-post With effect from 2001, the National Board of Health and Welfare classifies its publications into various types of document. This an Overview of Knowledge . That means that the report is based on science and/or proven experience. Overviews of knowledge among other things are to provide support for knowledge-based care and treatment, method development and other improvement work, encourage and facilitate quality follow-up and/or encourage efficient utilisation of resources. The National Board of Health and Welfare is responsible for the contents and conclusions. Hypohidrotic Ectodermal Dysplasia Ectodermal dysplasia Anhidrotic Ectodermal Dysplasia EDA I Christ-Siemens-Touraine Syndrome Table of Contents The disease/injury/diagnosis Incidence Aetiology of the disease/injury Heredity ... Database references Document date : 2002-04-29 Version 1:0 Article number: 2002-110-10 English index Search The aphabetical list This is an excerpt from the knowledge database of the Swedish National Board of Health and Welfare on rare diseases. The concept of "rare diseases" is defined as: "Disorders or injuries resulting in extensive handicaps and affecting no more than 100 individuals in one million inhabitants". The ambition underlying the database is to provide up-to-date information on rare diseases and about the support and services these groups of people require. The disease/injury/diagnosis Hypohidrotic ectodermal dysplasia, ectodermal dysplasia, anhidrotic ectodermal dysplasia (EDA I), Christ-Siemens-Touraine Syndrome.

56. ECTODERMAL DYSPLASIA RappHodgkin Syndrome,Hypohidrotic ectodermal dysplasia autosomal Rapp-Hodgkin Syndrome,Hypohidrotic ectodermal dysplasia autosomal dominant type,RHS,ectodermal dysplasia anhidrotic with cleft lip and cleft palate,Ectodermal http://www.websters-online-dictionary.org/definition/english/Ec/Ectodermal Dyspl

Philip M. Parker, INSEAD. ECTODERMAL DYSPLASIA Specialty Definition: ECTODERMAL DYSPLASIA Domain Definition Health A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of abnormalities at birth and involvement of both the epidermis and skin appendages. They are generally nonprogressive and diffuse. Various forms exist, including anhidrotic and hidrotic dysplasias, focal dermal hypoplasia, and aplasia cutis congenita. ( references Source: compiled by the editor from various references ; see credits. Top Frequency of Internet Keywords: ECTODERMAL DYSPLASIA The following statistics estimate the number of searches per day across the major English-language search engines as identified by various trade publications. Hyperlinks lead to commercial use of the expression at Amazon.com Expression Frequency per Day ectodermal dysplasia Source: compiled by the editor from various references ; see credits. Top Modern Translation: ECTODERMAL DYSPLASIA Language Translations for "ECTODERMAL DYSPLASIA"; alternative meanings/domain in parentheses.

57. Hypohidrotic Ectodermal Dysplasia,HED,Anhidrotic Ectodermal Dysplasia,EDA,Christ Hypohidrotic ectodermal dysplasia,HED,Anhidrotic ectodermal dysplasia,EDA,ChristSiemens-Touraine Syndrome,CST Syndrome,Hypohidrotic ectodermal dysplasia,HED http://www.icomm.ca/geneinfo/hed.htm

Hypohidrotic Ectodermal Dysplasia,HED,Anhidrotic Ectodermal Dysplasia,EDA,Christ-Siemens-Touraine Syndrome,CST Syndrome,Hypohidrotic Ectodermal Dysplasia,HED,Anhidrotic Ectodermal Dysplasia,EDA,Christ-Siemens-Touraine Syndrome,CST Syndrome For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX to Information on the Internet about Genetic Disorders and Birth Defects Genetic Information and Patient Services, Inc. (GAPS) HOME DISORDERS GLOSSARY Hypohidrotic Ectodermal Dysplasia (as defined by the National Organization for Rare Disorders also known as: HED Anhidrotic Ectodermal Dysplasia EDA Christ-Siemens-Touraine Syndrome CST Syndrome Hypohidrotic ectodermal dysplasia (HED) is a rare inherited multisystem disorder that belongs to the group of diseases known as ectodermal dysplasias. Ectodermal dysplasias typically affect the hair, teeth, nails, and/or skin. HED is primarily characterized by partial or complete absence of certain sweat glands (eccrine glands), causing lack of or diminished sweating (anhidrosis or hypohidrosis), heat intolerance, and fever; abnormally sparse hair (hypotrichosis); and absence (hypodontia) and/or malformation of certain teeth. Many individuals with HED also have characteristic facial abnormalities including a prominent forehead, a sunken nasal bridge (so-called "saddle nose"), unusually thick lips, and/or a large chin.

58. Health Topics ectodermal dysplasia. Definition Ectodermal Alternative Names Anhidrotic ectodermal dysplasia. Causes, incidence, and risk factors There http://www.netwellness.org/ency/article/001469.htm

How to Use the Information Search Ask an Expert ... Prevention Ectodermal dysplasia Definition: Ectodermal dysplasia is a hereditary condition characterized by abnormal development of the skin and associated structures (hair, nails and teeth, and sweat glands). Alternative Names: Anhidrotic ectodermal dysplasia Causes, incidence, and risk factors: There are many different types of ectodermal dysplasia of which X-linked anhidrotic ectodermal dysplasia is the most common. Because the disease is X-linked, males are affected, although females in some cases may also display a range of symptoms. An autosomal dominant form exists in which females and males are equally affected and is symptomatically almost identical to the X-linked form of the disease. Multiple genes have been discovered to cause ectodermal dysplasias. Ectodermal dysplasia may affect, to varying degrees, all of the structures associated with the development of the skin. Absent or decreased sweating in people with anhidrotic ectodermal dysplasia is caused by absence of sweat glands. Affected children have difficulty controlling fevers and mild illness may produce extremely high fevers, because of absent temperature regulation by

59. Disease - Ectodermal Dysplasia - Hartford, Connecticut , Saint Francis Care Disease ectodermal dysplasia - courtesy of Saint Francis Care of Hartford, Connecticut, contemporary medicine with major clinical concentrations in heart http://www.saintfranciscare.com/11875.cfm

@import url(main.css); About Us Health Information Adam Article Manager CareMail Signup ... Ways To Help Adam Article Manager Back Back to main Health Information page Disease - Ectodermal dysplasia Skin layers Definition: Ectodermal dysplasia is a hereditary condition characterized by abnormal development of the skin and associated structures (hair, nails and teeth, and sweat glands). Alternative Names: Anhidrotic ectodermal dysplasia Causes And Risk: There are many different types of ectodermal dysplasia of which X-linked anhidrotic ectodermal dysplasia is the most common. Because the disease is X-linked, males are affected, although females in some cases may also display a range of symptoms. An autosomal dominant form exists in which females and males are equally affected and is symptomatically almost identical to the X-linked form of the disease. Multiple genes have been discovered to cause ectodermal dysplasias. Ectodermal dysplasia may affect, to varying degrees, all of the structures associated with the development of the skin. Absent or decreased sweating in people with anhidrotic ectodermal dysplasia is caused by absence of sweat glands.

60. Hereditary Anhidrotic Ectodermal Dysplasia Hereditary anhidrotic ectodermal dysplasia. Siemens syndrome. ICD9-CM 757.31 congenital ectodermal dysplasia Author(s) Mark R. Dambro, MD http://www.5mcc.com/Assets/SUMMARY/TP0418.html

Hereditary anhidrotic ectodermal dysplasia DESCRIPTION: A congenital ectodermal defect that is x-linked recessive; autosomal recessive. Only males fully express the condition; female carriers may have mild symptoms in x-linked recessive form; both sexes equally affected in autosomal recessive form. Symptoms: heat intolerance, facial anomalies, anhidrosis, hypotrichosis, short stature, dry skin, no mammary glands, mental retardation. Chronic course. CAUSES: defective ectodermal structures inherited disease Synonyms: Christ-Siemens-Touraine syndrome Siemens syndrome ICD-9-CM: 757.31 congenital ectodermal dysplasia Author(s): Mark R. Dambro, MD

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