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Complete Androgen Insensitivity Syndrome: Dilemmas for Further Management after Gonadectomy

Complete androgen insensitivity syndrome is a rare condition, wherein a genetic male is phenotypically female and is raised as a female. Treatement requires timely gonadectomy, need for long term hormonal replaceent therapy, psycological and genetic counseling. The type, dose, duration of hrt is not...

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Autores principales: Singh, Pratibha, Gothwal, Meenakshi, Yadav, Garima, Singh, Kuldeep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937775/
https://www.ncbi.nlm.nih.gov/pubmed/32038088
http://dx.doi.org/10.4103/jhrs.JHRS_151_18
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author Singh, Pratibha
Gothwal, Meenakshi
Yadav, Garima
Singh, Kuldeep
author_facet Singh, Pratibha
Gothwal, Meenakshi
Yadav, Garima
Singh, Kuldeep
author_sort Singh, Pratibha
collection PubMed
description Complete androgen insensitivity syndrome is a rare condition, wherein a genetic male is phenotypically female and is raised as a female. Treatement requires timely gonadectomy, need for long term hormonal replaceent therapy, psycological and genetic counseling. The type, dose, duration of hrt is not well studied. Reproductive issues also need to be addressed in these young woman. We report here a case of complete androgen insensitivity which posed a quandary for management of long term bone health. Review of literature for management is discussed. These cases are best managed by a multi-disciplenary team comprising of gynecologist, geneticist, endocrinologist and clinical psycologist or psychiatrist.
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spelling pubmed-69377752020-02-07 Complete Androgen Insensitivity Syndrome: Dilemmas for Further Management after Gonadectomy Singh, Pratibha Gothwal, Meenakshi Yadav, Garima Singh, Kuldeep J Hum Reprod Sci Case Report Complete androgen insensitivity syndrome is a rare condition, wherein a genetic male is phenotypically female and is raised as a female. Treatement requires timely gonadectomy, need for long term hormonal replaceent therapy, psycological and genetic counseling. The type, dose, duration of hrt is not well studied. Reproductive issues also need to be addressed in these young woman. We report here a case of complete androgen insensitivity which posed a quandary for management of long term bone health. Review of literature for management is discussed. These cases are best managed by a multi-disciplenary team comprising of gynecologist, geneticist, endocrinologist and clinical psycologist or psychiatrist. Wolters Kluwer - Medknow 2019 2019-12-17 /pmc/articles/PMC6937775/ /pubmed/32038088 http://dx.doi.org/10.4103/jhrs.JHRS_151_18 Text en Copyright: © 2019 Journal of Human Reproductive Sciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Singh, Pratibha
Gothwal, Meenakshi
Yadav, Garima
Singh, Kuldeep
Complete Androgen Insensitivity Syndrome: Dilemmas for Further Management after Gonadectomy
title Complete Androgen Insensitivity Syndrome: Dilemmas for Further Management after Gonadectomy
title_full Complete Androgen Insensitivity Syndrome: Dilemmas for Further Management after Gonadectomy
title_fullStr Complete Androgen Insensitivity Syndrome: Dilemmas for Further Management after Gonadectomy
title_full_unstemmed Complete Androgen Insensitivity Syndrome: Dilemmas for Further Management after Gonadectomy
title_short Complete Androgen Insensitivity Syndrome: Dilemmas for Further Management after Gonadectomy
title_sort complete androgen insensitivity syndrome: dilemmas for further management after gonadectomy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937775/
https://www.ncbi.nlm.nih.gov/pubmed/32038088
http://dx.doi.org/10.4103/jhrs.JHRS_151_18
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