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Thyroid abnormalities in children with Down syndrome at St. Paul's hospital millennium medical college, Ethiopia
BACKGROUND: Subclinical hypothyroidism (SCH) is the commonest thyroid abnormality in patients with Down syndrome (DS). The purpose of this study was to determine the prevalence and types of thyroid abnormalities, to assess the age at diagnosis, and to examine the screening practice in children with...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9094469/ https://www.ncbi.nlm.nih.gov/pubmed/35426257 http://dx.doi.org/10.1002/edm2.337 |
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author | Mulu, Birtukan Fantahun, Bereket |
author_facet | Mulu, Birtukan Fantahun, Bereket |
author_sort | Mulu, Birtukan |
collection | PubMed |
description | BACKGROUND: Subclinical hypothyroidism (SCH) is the commonest thyroid abnormality in patients with Down syndrome (DS). The purpose of this study was to determine the prevalence and types of thyroid abnormalities, to assess the age at diagnosis, and to examine the screening practice in children with DS in a resource limited setting. METHODOLOGY: A retrospective study was conducted in children with DS seen at endocrine follow‐up clinic. Data were collected from patients' registration book and medical records. RESULT: A total of 115 patients with DS were included in the study out of which 64 (59.8%) were males. Their median age at diagnosis was 9 months (range 4–15 years). Thyroid function test (TFT) was done at least once for 107 (93%) patients. Abnormal thyroid function was observed in 51 (47.7%) patients. The commonest thyroid abnormality was SCH (30/107, 28%) followed by congenital hypothyroidism (11/107, 10.3%), overt hypothyroidism (9/107, 8.4%) and hyperthyroidism (1/107, 0.9%). Most of the patients (86/107, 80.4%) were tested initially in the first 2 years of life. From those who were tested between the age of 2–6 months (n = 22 patients), seven (31.8%) patients had thyroid abnormalities. CONCLUSION: Thyroid abnormalities were seen in a remarkable proportion of DS patients. The detection of abnormalities in the patients with age range of 2–6 months demands the need for additional TFT in this age category apart from the standard recommendation. Early diagnosis and management of thyroid abnormalities are important to decrease further impairment of cognition function in children with DS. |
format | Online Article Text |
id | pubmed-9094469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90944692022-05-18 Thyroid abnormalities in children with Down syndrome at St. Paul's hospital millennium medical college, Ethiopia Mulu, Birtukan Fantahun, Bereket Endocrinol Diabetes Metab Research Articles BACKGROUND: Subclinical hypothyroidism (SCH) is the commonest thyroid abnormality in patients with Down syndrome (DS). The purpose of this study was to determine the prevalence and types of thyroid abnormalities, to assess the age at diagnosis, and to examine the screening practice in children with DS in a resource limited setting. METHODOLOGY: A retrospective study was conducted in children with DS seen at endocrine follow‐up clinic. Data were collected from patients' registration book and medical records. RESULT: A total of 115 patients with DS were included in the study out of which 64 (59.8%) were males. Their median age at diagnosis was 9 months (range 4–15 years). Thyroid function test (TFT) was done at least once for 107 (93%) patients. Abnormal thyroid function was observed in 51 (47.7%) patients. The commonest thyroid abnormality was SCH (30/107, 28%) followed by congenital hypothyroidism (11/107, 10.3%), overt hypothyroidism (9/107, 8.4%) and hyperthyroidism (1/107, 0.9%). Most of the patients (86/107, 80.4%) were tested initially in the first 2 years of life. From those who were tested between the age of 2–6 months (n = 22 patients), seven (31.8%) patients had thyroid abnormalities. CONCLUSION: Thyroid abnormalities were seen in a remarkable proportion of DS patients. The detection of abnormalities in the patients with age range of 2–6 months demands the need for additional TFT in this age category apart from the standard recommendation. Early diagnosis and management of thyroid abnormalities are important to decrease further impairment of cognition function in children with DS. John Wiley and Sons Inc. 2022-04-14 /pmc/articles/PMC9094469/ /pubmed/35426257 http://dx.doi.org/10.1002/edm2.337 Text en © 2022 The Authors. Endocrinology, Diabetes & Metabolism published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Mulu, Birtukan Fantahun, Bereket Thyroid abnormalities in children with Down syndrome at St. Paul's hospital millennium medical college, Ethiopia |
title | Thyroid abnormalities in children with Down syndrome at St. Paul's hospital millennium medical college, Ethiopia |
title_full | Thyroid abnormalities in children with Down syndrome at St. Paul's hospital millennium medical college, Ethiopia |
title_fullStr | Thyroid abnormalities in children with Down syndrome at St. Paul's hospital millennium medical college, Ethiopia |
title_full_unstemmed | Thyroid abnormalities in children with Down syndrome at St. Paul's hospital millennium medical college, Ethiopia |
title_short | Thyroid abnormalities in children with Down syndrome at St. Paul's hospital millennium medical college, Ethiopia |
title_sort | thyroid abnormalities in children with down syndrome at st. paul's hospital millennium medical college, ethiopia |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9094469/ https://www.ncbi.nlm.nih.gov/pubmed/35426257 http://dx.doi.org/10.1002/edm2.337 |
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