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Clinical Spectrum of Disorders of Sex Development: A Cross-sectional Observational Study
OBJECTIVE: Disorders of sex development (DSD) constitutes a small but difficult and equally important area of endocrinology. It is often a social emergency as the decision regarding sex assignment in these cases is extremely disturbing and difficult to both families and healthcare professionals. Our...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330871/ https://www.ncbi.nlm.nih.gov/pubmed/30766817 http://dx.doi.org/10.4103/ijem.IJEM_159_18 |
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author | Dar, Sheeraz A. Nazir, Mudasir Lone, Roumissa Sameen, Duri Ahmad, Ikhlas Wani, Wasim A. Charoo, Bashir A. |
author_facet | Dar, Sheeraz A. Nazir, Mudasir Lone, Roumissa Sameen, Duri Ahmad, Ikhlas Wani, Wasim A. Charoo, Bashir A. |
author_sort | Dar, Sheeraz A. |
collection | PubMed |
description | OBJECTIVE: Disorders of sex development (DSD) constitutes a small but difficult and equally important area of endocrinology. It is often a social emergency as the decision regarding sex assignment in these cases is extremely disturbing and difficult to both families and healthcare professionals. Our study was devised to assess the clinical and chromosomal profile of patients with suspected DSD and classify them according to the new DSD consensus document. SUBJECTS AND METHODS: This study was a cross-sectional observational study carried out in the department of pediatrics of a tertiary care hospital from August 2012 to August 2014. All patients with suspected DSD in the age group of 0–19 years were included. After detailed history and examination, karyotyping, abdominal sonography, and hormonal analysis were done. Additional studies like gonadal biopsy, laparoscopy, and hormone stimulation tests were done in selected cases. RESULTS: About 41 patients were included in the study. The mean age of presentation was 87 months (1 day to 16 years). Only seven (13.7%) patients presented in neonatal period. In total, 25 patients had ambiguous genitalia; 46, XX DSD were diagnosed in 24 (58.5%) patients, 46, XY DSD in 10 (24.4%) patients, and sex chromosome DSD in 7 (17.1%). Congenital adrenal hyperplasia (CAH) was the commonest disease diagnosed in 21 (51.2%) patients. Turner syndrome, Klinefelter syndrome, androgen insensitivity syndrome, 46, XX ovotesticular disorder, and 46, XY gonadal dysgenesis were diagnosed in 3, 3, 4, 3, and 5 patients, respectively. Eleven patients with CAH presented in shock and six had history of sib deaths. CONCLUSION: 46, XX DSD were the commonest etiological group in our study and CAH was the commonest individual disease. There is a need for educating general public and practitioners regarding DSD to allow early intervention. Moreover, there is a need to introduce routine neonatal screening for CAH in our country. |
format | Online Article Text |
id | pubmed-6330871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63308712019-02-14 Clinical Spectrum of Disorders of Sex Development: A Cross-sectional Observational Study Dar, Sheeraz A. Nazir, Mudasir Lone, Roumissa Sameen, Duri Ahmad, Ikhlas Wani, Wasim A. Charoo, Bashir A. Indian J Endocrinol Metab Original Article OBJECTIVE: Disorders of sex development (DSD) constitutes a small but difficult and equally important area of endocrinology. It is often a social emergency as the decision regarding sex assignment in these cases is extremely disturbing and difficult to both families and healthcare professionals. Our study was devised to assess the clinical and chromosomal profile of patients with suspected DSD and classify them according to the new DSD consensus document. SUBJECTS AND METHODS: This study was a cross-sectional observational study carried out in the department of pediatrics of a tertiary care hospital from August 2012 to August 2014. All patients with suspected DSD in the age group of 0–19 years were included. After detailed history and examination, karyotyping, abdominal sonography, and hormonal analysis were done. Additional studies like gonadal biopsy, laparoscopy, and hormone stimulation tests were done in selected cases. RESULTS: About 41 patients were included in the study. The mean age of presentation was 87 months (1 day to 16 years). Only seven (13.7%) patients presented in neonatal period. In total, 25 patients had ambiguous genitalia; 46, XX DSD were diagnosed in 24 (58.5%) patients, 46, XY DSD in 10 (24.4%) patients, and sex chromosome DSD in 7 (17.1%). Congenital adrenal hyperplasia (CAH) was the commonest disease diagnosed in 21 (51.2%) patients. Turner syndrome, Klinefelter syndrome, androgen insensitivity syndrome, 46, XX ovotesticular disorder, and 46, XY gonadal dysgenesis were diagnosed in 3, 3, 4, 3, and 5 patients, respectively. Eleven patients with CAH presented in shock and six had history of sib deaths. CONCLUSION: 46, XX DSD were the commonest etiological group in our study and CAH was the commonest individual disease. There is a need for educating general public and practitioners regarding DSD to allow early intervention. Moreover, there is a need to introduce routine neonatal screening for CAH in our country. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6330871/ /pubmed/30766817 http://dx.doi.org/10.4103/ijem.IJEM_159_18 Text en Copyright: © 2018 Indian Journal of Endocrinology and Metabolism 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 | Original Article Dar, Sheeraz A. Nazir, Mudasir Lone, Roumissa Sameen, Duri Ahmad, Ikhlas Wani, Wasim A. Charoo, Bashir A. Clinical Spectrum of Disorders of Sex Development: A Cross-sectional Observational Study |
title | Clinical Spectrum of Disorders of Sex Development: A Cross-sectional Observational Study |
title_full | Clinical Spectrum of Disorders of Sex Development: A Cross-sectional Observational Study |
title_fullStr | Clinical Spectrum of Disorders of Sex Development: A Cross-sectional Observational Study |
title_full_unstemmed | Clinical Spectrum of Disorders of Sex Development: A Cross-sectional Observational Study |
title_short | Clinical Spectrum of Disorders of Sex Development: A Cross-sectional Observational Study |
title_sort | clinical spectrum of disorders of sex development: a cross-sectional observational study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330871/ https://www.ncbi.nlm.nih.gov/pubmed/30766817 http://dx.doi.org/10.4103/ijem.IJEM_159_18 |
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