Christ Siemen Touraine Syndrome - A Case Report
Christ Siemen Touraine Syndrome [CST syndrome] more commonly referred to as anhidrotic/hypohidrotic ectodermal dysplasia. It is a hereditary disorder characterized by abnormal development of certain tissues and structures of ectodermal origin. It is diffuse, nonprogressive disease characterized at b...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
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Wolters Kluwer Medknow Publications
2004-01-01
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| Series: | Journal of Indian Academy of Oral Medicine and Radiology |
| Subjects: | |
| Online Access: | http://www.jiaomr.in/article.asp?issn=0972-1363;year=2004;volume=16;issue=2;spage=137;epage=140;aulast=Indurkar;type=0 |
| _version_ | 1818402766198931456 |
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| author | A D Indurkar S S Degwekar R H Chole |
| author_facet | A D Indurkar S S Degwekar R H Chole |
| author_sort | A D Indurkar |
| collection | DOAJ |
| description | Christ Siemen Touraine Syndrome [CST syndrome] more commonly referred to as anhidrotic/hypohidrotic ectodermal dysplasia. It is a hereditary disorder characterized by abnormal development of certain tissues and structures of ectodermal origin. It is diffuse, nonprogressive disease characterized at birth and by involvement of epidermis plus atleast one of appendages (hair, sebaceous glands, nails, teeth or mucous glands). Hypotrichosis, hypodontia, hypohydrosis and occasional onychodysplasia are prominent features. It is an X-linked recessive disorder occurring in its full expression only in males, females as heterozygotes may be mildly affected.
A case of 20 year old male with CST syndrome is discussed in this article. |
| first_indexed | 2024-12-14T08:13:34Z |
| format | Article |
| id | doaj.art-b82eb461ad87430298558e030e115a62 |
| institution | Directory Open Access Journal |
| issn | 0972-1363 0975-1572 |
| language | English |
| last_indexed | 2024-12-14T08:13:34Z |
| publishDate | 2004-01-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | Journal of Indian Academy of Oral Medicine and Radiology |
| spelling | doaj.art-b82eb461ad87430298558e030e115a622022-12-21T23:10:00ZengWolters Kluwer Medknow PublicationsJournal of Indian Academy of Oral Medicine and Radiology0972-13630975-15722004-01-01162137140Christ Siemen Touraine Syndrome - A Case ReportA D IndurkarS S DegwekarR H CholeChrist Siemen Touraine Syndrome [CST syndrome] more commonly referred to as anhidrotic/hypohidrotic ectodermal dysplasia. It is a hereditary disorder characterized by abnormal development of certain tissues and structures of ectodermal origin. It is diffuse, nonprogressive disease characterized at birth and by involvement of epidermis plus atleast one of appendages (hair, sebaceous glands, nails, teeth or mucous glands). Hypotrichosis, hypodontia, hypohydrosis and occasional onychodysplasia are prominent features. It is an X-linked recessive disorder occurring in its full expression only in males, females as heterozygotes may be mildly affected. A case of 20 year old male with CST syndrome is discussed in this article.http://www.jiaomr.in/article.asp?issn=0972-1363;year=2004;volume=16;issue=2;spage=137;epage=140;aulast=Indurkar;type=0Syndromeectodermal dysplasia. |
| spellingShingle | A D Indurkar S S Degwekar R H Chole Christ Siemen Touraine Syndrome - A Case Report Journal of Indian Academy of Oral Medicine and Radiology Syndrome ectodermal dysplasia. |
| title | Christ Siemen Touraine Syndrome - A Case Report |
| title_full | Christ Siemen Touraine Syndrome - A Case Report |
| title_fullStr | Christ Siemen Touraine Syndrome - A Case Report |
| title_full_unstemmed | Christ Siemen Touraine Syndrome - A Case Report |
| title_short | Christ Siemen Touraine Syndrome - A Case Report |
| title_sort | christ siemen touraine syndrome a case report |
| topic | Syndrome ectodermal dysplasia. |
| url | http://www.jiaomr.in/article.asp?issn=0972-1363;year=2004;volume=16;issue=2;spage=137;epage=140;aulast=Indurkar;type=0 |
| work_keys_str_mv | AT adindurkar christsiementourainesyndromeacasereport AT ssdegwekar christsiementourainesyndromeacasereport AT rhchole christsiementourainesyndromeacasereport |