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         Ectodermal Dysplasia:     more books (15)
  1. Freire-Maia Ectodermal Dysplasias- A Clinical an D Genetic Study by N FREIRE-MAIA, 1985-02-06
  2. Ectrodactyly-ectodermal dysplasia-cleft syndrome
  3. Ectrodactyly-ectodermal dysplasia-clefting syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Kathleen, MS, CGC Fergus, 2005
  4. Children with ectodermal dysplasias.: An article from: Journal of School Health by Virginia L. Maturen, 1998-05-01
  5. Hypohidrotic Ectodermal Dysplasia - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-17
  6. ECTRODACTYLY-ECTODERMAL DYSPLASIA-CLEFTING SYNDROME IN AN INFANT WITH A VENTRICULAR SEPTAL DEFECT.: An article from: Georgia Journal of Science by Byron A. Brown, Joshua E. Lane, et all 2000-09-22
  7. Ectodermal dysplasia: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Jennifer, MS, CGC Roggenbuck, 2005
  8. Ectrodactyly-Ectodermal Dysplasia-Cleft Syndrome (EEC) Medical Guide by Qontro Medical Guides, 2008-07-09
  9. Oligodontia and ectodermal dysplasia - on signs, syptoms, genetics, and outcomes of dental treatment by Birgitta Bergendal, 2010-05
  10. Recent advances in ectodermal dysplasias (Birth defects, original article series)
  11. Recent Advances in Ectodermal Dysplasias (Birth Defects Original Article Series) by Carlos F. Salinas, John M. Opitz, 1988-09
  12. Charley's story by Mary Kaye Richter, 2000
  13. Adams-Oliver syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Amy, MS, CGC Vance, 2005
  14. Goltz syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Paul Johnson, 2005

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
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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 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:
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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 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
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  • 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
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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
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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
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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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