Complete Androgen Insensitivity Syndrome: A Rare Case of Disorder of Sex Development
Androgen Insensitivity Syndrome (AIS) could be considered as a disease that causes resistance to androgens actions, influencing both the morphogenesis and differentiation of the body structures, and systems in which this hormone exerts its effects. It depends on an X-linked mutations in the Androgen...
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Format: | Article |
Language: | English |
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Wiley
2013-01-01
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Series: | Case Reports in Obstetrics and Gynecology |
Online Access: | http://dx.doi.org/10.1155/2013/232696 |
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author | Alfonsa Pizzo Antonio Simone Laganà Irene Borrielli Nella Dugo |
author_facet | Alfonsa Pizzo Antonio Simone Laganà Irene Borrielli Nella Dugo |
author_sort | Alfonsa Pizzo |
collection | DOAJ |
description | Androgen Insensitivity Syndrome (AIS) could be considered as a disease that causes resistance to androgens actions, influencing both the morphogenesis and differentiation of the body structures, and systems in which this hormone exerts its effects. It depends on an X-linked mutations in the Androgen Receptor (AR) gene that express a variety of phenotypes ranging from male infertility to completely normal female external genitalia. The clinical phenotypes of AIS could vary and be classified into three categories, as complete (CAIS), partial (PAIS), and mild (MAIS) forms, according to the severity of androgen resistance. We will describe a case of CAIS in a 16-year-old patient. |
format | Article |
id | doaj-art-60804cd92021404b8dd6c28b12cac26c |
institution | Kabale University |
issn | 2090-6684 2090-6692 |
language | English |
publishDate | 2013-01-01 |
publisher | Wiley |
record_format | Article |
series | Case Reports in Obstetrics and Gynecology |
spelling | doaj-art-60804cd92021404b8dd6c28b12cac26c2025-02-03T06:14:18ZengWileyCase Reports in Obstetrics and Gynecology2090-66842090-66922013-01-01201310.1155/2013/232696232696Complete Androgen Insensitivity Syndrome: A Rare Case of Disorder of Sex DevelopmentAlfonsa Pizzo0Antonio Simone Laganà1Irene Borrielli2Nella Dugo3Department of Pediatric, Gynecological, Microbiological and Biomedical Sciences, University of Messina, Via C. Valeria 1, 98125 Messina, ItalyDepartment of Pediatric, Gynecological, Microbiological and Biomedical Sciences, University of Messina, Via C. Valeria 1, 98125 Messina, ItalyDepartment of Pediatric, Gynecological, Microbiological and Biomedical Sciences, University of Messina, Via C. Valeria 1, 98125 Messina, ItalyDepartment of Gynecology and Obstetrics, Campus Bio-Medico, Via Álvaro del Portillo 200, 00128 Roma, ItalyAndrogen Insensitivity Syndrome (AIS) could be considered as a disease that causes resistance to androgens actions, influencing both the morphogenesis and differentiation of the body structures, and systems in which this hormone exerts its effects. It depends on an X-linked mutations in the Androgen Receptor (AR) gene that express a variety of phenotypes ranging from male infertility to completely normal female external genitalia. The clinical phenotypes of AIS could vary and be classified into three categories, as complete (CAIS), partial (PAIS), and mild (MAIS) forms, according to the severity of androgen resistance. We will describe a case of CAIS in a 16-year-old patient.http://dx.doi.org/10.1155/2013/232696 |
spellingShingle | Alfonsa Pizzo Antonio Simone Laganà Irene Borrielli Nella Dugo Complete Androgen Insensitivity Syndrome: A Rare Case of Disorder of Sex Development Case Reports in Obstetrics and Gynecology |
title | Complete Androgen Insensitivity Syndrome: A Rare Case of Disorder of Sex Development |
title_full | Complete Androgen Insensitivity Syndrome: A Rare Case of Disorder of Sex Development |
title_fullStr | Complete Androgen Insensitivity Syndrome: A Rare Case of Disorder of Sex Development |
title_full_unstemmed | Complete Androgen Insensitivity Syndrome: A Rare Case of Disorder of Sex Development |
title_short | Complete Androgen Insensitivity Syndrome: A Rare Case of Disorder of Sex Development |
title_sort | complete androgen insensitivity syndrome a rare case of disorder of sex development |
url | http://dx.doi.org/10.1155/2013/232696 |
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