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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Main Authors: Alfonsa Pizzo, Antonio Simone Laganà, Irene Borrielli, Nella Dugo
Format: Article
Language:English
Published: Wiley 2013-01-01
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.
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institution Kabale University
issn 2090-6684
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publishDate 2013-01-01
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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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