Caracterização das crianças com síndrome de Down concomitante ao hipotireoidismo congênito no estado de Mato Grosso, Região Central do Brasil, 2010–2021
OBJECTIVE: Congenital hypothyroidism is a frequent disease in pediatric endocrinology, with a high prevalence among children with Down syndrome. In Brazil, publications on the coexistence of these two syndromes in children are scarce. The aim of this study was to clinically and laboratory characteri...
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Sociedade Brasileira de Pediatria
2024-12-01
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Series: | Residência Pediátrica |
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Online Access: | https://cdn.publisher.gn1.link/residenciapediatrica.com.br/pdf/v14n4a1167.pdf |
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author | Camila Moraes Mello Stela Maris Silvestrin |
author_facet | Camila Moraes Mello Stela Maris Silvestrin |
author_sort | Camila Moraes Mello |
collection | DOAJ |
description | OBJECTIVE: Congenital hypothyroidism is a frequent disease in pediatric endocrinology, with a high prevalence among children with Down syndrome. In Brazil, publications on the coexistence of these two syndromes in children are scarce. The aim of this study was to clinically and laboratory characterize children with Down syndrome concomitant with congenital hypothyroidism.
METHODOLOGY: This is a cross-sectional and retrospective study with data from medical records of patients with Down syndrome concomitant with congenital hypothyroidism among live births from January 2010 to December 2021, followed at a neonatal screening service in Mato Grosso, Brazil.
RESULTS: 318 children with congenital hypothyroidism were analyzed, 11 of them with Down syndrome (prevalence of 1:28.9 among children with congenital hypothyroidism). The most common clinical finding was jaundice (90.0%), followed by macroglossia (80.0%), hypotonia (66.7%) and livedo reticularis (62.5%). Congenital cardiac anomalies occurred in all children with Down syndrome studied. Interatrial communication and patent ductus arteriosus were the most frequent cardiac anomalies. Serum levels of thyrotropin were between 10 µIU/mL and 20 µIU/mL in 63.6% of the sample and in two patients, these values ??were above 100 µIU/mL. In 81.8% of the children, free thyroxine levels were normal. The absolute majority of children did not show thyroid ultrasonographic alteration.
CONCLUSIONS: A high prevalence of Down syndrome was observed among patients with congenital hypothyroidism, with the subclinical form of hypothyroidism being the most common presentation. Jaundice, macroglossia and congenital heart disease were the most relevant clinical findings in this study. |
format | Article |
id | doaj-art-3d10500a1e7c4d7f881c75ec0cd1c587 |
institution | Kabale University |
issn | 2236-6814 |
language | English |
publishDate | 2024-12-01 |
publisher | Sociedade Brasileira de Pediatria |
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series | Residência Pediátrica |
spelling | doaj-art-3d10500a1e7c4d7f881c75ec0cd1c5872025-01-06T13:54:01ZengSociedade Brasileira de PediatriaResidência Pediátrica2236-68142024-12-0114410.25060/residpediatr-2024.v14n4-1167Caracterização das crianças com síndrome de Down concomitante ao hipotireoidismo congênito no estado de Mato Grosso, Região Central do Brasil, 2010–2021Camila Moraes Mello0Stela Maris Silvestrin1Universidade Federal de Mato Grosso, Departamento de Pediatria - Hospital Universitário Júlio Müller - Cuiabá - Mato Grosso - BrasilUniversidade Federal de Mato Grosso, Departamento de Pediatria - Hospital Universitário Júlio Müller - Cuiabá - Mato Grosso - BrasilOBJECTIVE: Congenital hypothyroidism is a frequent disease in pediatric endocrinology, with a high prevalence among children with Down syndrome. In Brazil, publications on the coexistence of these two syndromes in children are scarce. The aim of this study was to clinically and laboratory characterize children with Down syndrome concomitant with congenital hypothyroidism. METHODOLOGY: This is a cross-sectional and retrospective study with data from medical records of patients with Down syndrome concomitant with congenital hypothyroidism among live births from January 2010 to December 2021, followed at a neonatal screening service in Mato Grosso, Brazil. RESULTS: 318 children with congenital hypothyroidism were analyzed, 11 of them with Down syndrome (prevalence of 1:28.9 among children with congenital hypothyroidism). The most common clinical finding was jaundice (90.0%), followed by macroglossia (80.0%), hypotonia (66.7%) and livedo reticularis (62.5%). Congenital cardiac anomalies occurred in all children with Down syndrome studied. Interatrial communication and patent ductus arteriosus were the most frequent cardiac anomalies. Serum levels of thyrotropin were between 10 µIU/mL and 20 µIU/mL in 63.6% of the sample and in two patients, these values ??were above 100 µIU/mL. In 81.8% of the children, free thyroxine levels were normal. The absolute majority of children did not show thyroid ultrasonographic alteration. CONCLUSIONS: A high prevalence of Down syndrome was observed among patients with congenital hypothyroidism, with the subclinical form of hypothyroidism being the most common presentation. Jaundice, macroglossia and congenital heart disease were the most relevant clinical findings in this study.https://cdn.publisher.gn1.link/residenciapediatrica.com.br/pdf/v14n4a1167.pdfcongenital hypothyroidismdown syndromeneonatal screeningthyrotropin |
spellingShingle | Camila Moraes Mello Stela Maris Silvestrin Caracterização das crianças com síndrome de Down concomitante ao hipotireoidismo congênito no estado de Mato Grosso, Região Central do Brasil, 2010–2021 Residência Pediátrica congenital hypothyroidism down syndrome neonatal screening thyrotropin |
title | Caracterização das crianças com síndrome de Down concomitante ao hipotireoidismo congênito no estado de Mato Grosso, Região Central do Brasil, 2010–2021 |
title_full | Caracterização das crianças com síndrome de Down concomitante ao hipotireoidismo congênito no estado de Mato Grosso, Região Central do Brasil, 2010–2021 |
title_fullStr | Caracterização das crianças com síndrome de Down concomitante ao hipotireoidismo congênito no estado de Mato Grosso, Região Central do Brasil, 2010–2021 |
title_full_unstemmed | Caracterização das crianças com síndrome de Down concomitante ao hipotireoidismo congênito no estado de Mato Grosso, Região Central do Brasil, 2010–2021 |
title_short | Caracterização das crianças com síndrome de Down concomitante ao hipotireoidismo congênito no estado de Mato Grosso, Região Central do Brasil, 2010–2021 |
title_sort | caracterizacao das criancas com sindrome de down concomitante ao hipotireoidismo congenito no estado de mato grosso regiao central do brasil 2010 2021 |
topic | congenital hypothyroidism down syndrome neonatal screening thyrotropin |
url | https://cdn.publisher.gn1.link/residenciapediatrica.com.br/pdf/v14n4a1167.pdf |
work_keys_str_mv | AT camilamoraesmello caracterizacaodascriancascomsindromededownconcomitanteaohipotireoidismocongenitonoestadodematogrossoregiaocentraldobrasil20102021 AT stelamarissilvestrin caracterizacaodascriancascomsindromededownconcomitanteaohipotireoidismocongenitonoestadodematogrossoregiaocentraldobrasil20102021 |