Management of Ectodermal Dysplasia in A 7 Year Old Child
Background: Ectodermal dysplasia is a hereditary group of disorders which are manifested as X-linked recessive trait and has a full expression in males, whereas females show little or no signs of the disorder. This disorder leads to disturbances in the ectoderm of the developing embryo. It has many...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
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Wolters Kluwer Medknow Publications
2016-01-01
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| Series: | Advances in Human Biology |
| Subjects: | |
| Online Access: | http://www.aihbonline.com/article.asp?issn=2321-8568;year=2016;volume=6;issue=1;spage=61;epage=64;aulast=Dave;type=0 |
| _version_ | 1811273682684739584 |
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| author | Bhavna Dave Devanshi Mehta Pratik B Kariya Keyur Joshi |
| author_facet | Bhavna Dave Devanshi Mehta Pratik B Kariya Keyur Joshi |
| author_sort | Bhavna Dave |
| collection | DOAJ |
| description | Background: Ectodermal dysplasia is a hereditary group of disorders which are manifested as X-linked recessive trait and has a full expression in males, whereas females show little or no signs of the disorder. This disorder leads to disturbances in the ectoderm of the developing embryo. It has many evident general and oral features which makes its rehabilitation of utmost importance. Correction of the presenting clinical oral disorders may help improve the quality of life for the patient. A multidisciplinary approach has to be adopted for such cases and it becomes a challenge in pediatric patients. In this report, etiology, clinical presentation, diagnosis and treatment plan of a 7-year-old male patient suffering from ectodermal dysplasia has been discussed. |
| first_indexed | 2024-04-12T23:03:40Z |
| format | Article |
| id | doaj.art-98ef807863354ccfbee8a00759451550 |
| institution | Directory Open Access Journal |
| issn | 2321-8568 2348-4691 |
| language | English |
| last_indexed | 2024-04-12T23:03:40Z |
| publishDate | 2016-01-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | Advances in Human Biology |
| spelling | doaj.art-98ef807863354ccfbee8a007594515502022-12-22T03:12:58ZengWolters Kluwer Medknow PublicationsAdvances in Human Biology2321-85682348-46912016-01-01616164Management of Ectodermal Dysplasia in A 7 Year Old ChildBhavna DaveDevanshi MehtaPratik B KariyaKeyur JoshiBackground: Ectodermal dysplasia is a hereditary group of disorders which are manifested as X-linked recessive trait and has a full expression in males, whereas females show little or no signs of the disorder. This disorder leads to disturbances in the ectoderm of the developing embryo. It has many evident general and oral features which makes its rehabilitation of utmost importance. Correction of the presenting clinical oral disorders may help improve the quality of life for the patient. A multidisciplinary approach has to be adopted for such cases and it becomes a challenge in pediatric patients. In this report, etiology, clinical presentation, diagnosis and treatment plan of a 7-year-old male patient suffering from ectodermal dysplasia has been discussed.http://www.aihbonline.com/article.asp?issn=2321-8568;year=2016;volume=6;issue=1;spage=61;epage=64;aulast=Dave;type=0DentistryEctodermal dysplasiaGenetic. |
| spellingShingle | Bhavna Dave Devanshi Mehta Pratik B Kariya Keyur Joshi Management of Ectodermal Dysplasia in A 7 Year Old Child Advances in Human Biology Dentistry Ectodermal dysplasia Genetic. |
| title | Management of Ectodermal Dysplasia in A 7 Year Old Child |
| title_full | Management of Ectodermal Dysplasia in A 7 Year Old Child |
| title_fullStr | Management of Ectodermal Dysplasia in A 7 Year Old Child |
| title_full_unstemmed | Management of Ectodermal Dysplasia in A 7 Year Old Child |
| title_short | Management of Ectodermal Dysplasia in A 7 Year Old Child |
| title_sort | management of ectodermal dysplasia in a 7 year old child |
| topic | Dentistry Ectodermal dysplasia Genetic. |
| url | http://www.aihbonline.com/article.asp?issn=2321-8568;year=2016;volume=6;issue=1;spage=61;epage=64;aulast=Dave;type=0 |
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