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Causes of short stature in Pakistani children found at an Endocrine Center
BACKGROUND AND OBJECTIVE: Short stature is defined as height below 3(rd) centile. Causes of short stature can range from familial, endocrine disorders, chronic diseases to chromosomal disorders. Most common cause in literature being idiopathic short stature. Early detection and management of remedia...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Professional Medical Publications
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216274/ https://www.ncbi.nlm.nih.gov/pubmed/28083018 http://dx.doi.org/10.12669/pjms.326.11077 |
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author | Jawa, Ali Riaz, Syed Hunain Khan Assir, Muhammad Zaman Afreen, Bahjat Riaz, Amna Akram, Javed |
author_facet | Jawa, Ali Riaz, Syed Hunain Khan Assir, Muhammad Zaman Afreen, Bahjat Riaz, Amna Akram, Javed |
author_sort | Jawa, Ali |
collection | PubMed |
description | BACKGROUND AND OBJECTIVE: Short stature is defined as height below 3(rd) centile. Causes of short stature can range from familial, endocrine disorders, chronic diseases to chromosomal disorders. Most common cause in literature being idiopathic short stature. Early detection and management of remedial disorders like malnutrition and vitamin D deficiency, Endocrine disorders like growth hormone deficiency & hypothyroidism can lead to attainment of expected height. Pakistani data shows idiopathic short stature as the most common cause of short stature. Our study aimed at detecting causes of short stature in children/adolescents at an Endocrine referral center. METHODS: A retrospective study was conducted at WILCARE Center for Diabetes, Endocrinology & Metabolism, Lahore on 70 well-nourished children/adolescents. The patients had been evaluated clinically, biochemically and radiologically as needed. Biochemical testing included hormonal testing as well to detect endocrine causes. Data was entered and analyzed in SPSS 20.0. RESULTS: Leading cause of short stature in our population was Growth Hormone (GH) deficiency seen in 48 out of 70 (69%) patients. Second most common endocrine abnormality seen in these patients was Vitamin D deficiency [44 out of 70 patients (63%)]. Primary hypothyroidism; pan-hypopituitarism & adrenal insufficiency were other endocrine causes. The weight for age was below 3(rd) percentile in 57 (81%) patients, with no association with other major causes. CONCLUSION: Growth hormone and Vitamin D deficiency constitute one of the major causes of short stature among well-nourished children with short stature in Pakistan. |
format | Online Article Text |
id | pubmed-5216274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Professional Medical Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-52162742017-01-12 Causes of short stature in Pakistani children found at an Endocrine Center Jawa, Ali Riaz, Syed Hunain Khan Assir, Muhammad Zaman Afreen, Bahjat Riaz, Amna Akram, Javed Pak J Med Sci Original Article BACKGROUND AND OBJECTIVE: Short stature is defined as height below 3(rd) centile. Causes of short stature can range from familial, endocrine disorders, chronic diseases to chromosomal disorders. Most common cause in literature being idiopathic short stature. Early detection and management of remedial disorders like malnutrition and vitamin D deficiency, Endocrine disorders like growth hormone deficiency & hypothyroidism can lead to attainment of expected height. Pakistani data shows idiopathic short stature as the most common cause of short stature. Our study aimed at detecting causes of short stature in children/adolescents at an Endocrine referral center. METHODS: A retrospective study was conducted at WILCARE Center for Diabetes, Endocrinology & Metabolism, Lahore on 70 well-nourished children/adolescents. The patients had been evaluated clinically, biochemically and radiologically as needed. Biochemical testing included hormonal testing as well to detect endocrine causes. Data was entered and analyzed in SPSS 20.0. RESULTS: Leading cause of short stature in our population was Growth Hormone (GH) deficiency seen in 48 out of 70 (69%) patients. Second most common endocrine abnormality seen in these patients was Vitamin D deficiency [44 out of 70 patients (63%)]. Primary hypothyroidism; pan-hypopituitarism & adrenal insufficiency were other endocrine causes. The weight for age was below 3(rd) percentile in 57 (81%) patients, with no association with other major causes. CONCLUSION: Growth hormone and Vitamin D deficiency constitute one of the major causes of short stature among well-nourished children with short stature in Pakistan. Professional Medical Publications 2016 /pmc/articles/PMC5216274/ /pubmed/28083018 http://dx.doi.org/10.12669/pjms.326.11077 Text en Copyright: © Pakistan Journal of Medical Sciences http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Jawa, Ali Riaz, Syed Hunain Khan Assir, Muhammad Zaman Afreen, Bahjat Riaz, Amna Akram, Javed Causes of short stature in Pakistani children found at an Endocrine Center |
title | Causes of short stature in Pakistani children found at an Endocrine Center |
title_full | Causes of short stature in Pakistani children found at an Endocrine Center |
title_fullStr | Causes of short stature in Pakistani children found at an Endocrine Center |
title_full_unstemmed | Causes of short stature in Pakistani children found at an Endocrine Center |
title_short | Causes of short stature in Pakistani children found at an Endocrine Center |
title_sort | causes of short stature in pakistani children found at an endocrine center |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216274/ https://www.ncbi.nlm.nih.gov/pubmed/28083018 http://dx.doi.org/10.12669/pjms.326.11077 |
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