Rickets vitamin-D-dependent type 2.
Autor(a) principal: | |
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Data de Publicação: | 2009 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1723 |
Resumo: | Rickets is a rare child disease especially in developed countries. Nutritional rickets remains the most prevalent condition, although congenital forms are well known. In the latest group, vitamin D dependent rickets type II is the rarest form and it can course with or without alopecia. There is a mutation on the receptor for vitamin D, with peripheral resistance to the vitamin D action. The authors present two clinical cases of vitamin D dependent rickets type II, in which the alopecia was a peculiar clinical sign that allowed the diagnoses. With prolonged calcium infusions, we achieved normal seric levels of calcium and correct bone disorders; alopecia persisted. This treatment is the most effective way to control the disease. |
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Rickets vitamin-D-dependent type 2.Raquitismo vitamina D dependente tipo II.Rickets is a rare child disease especially in developed countries. Nutritional rickets remains the most prevalent condition, although congenital forms are well known. In the latest group, vitamin D dependent rickets type II is the rarest form and it can course with or without alopecia. There is a mutation on the receptor for vitamin D, with peripheral resistance to the vitamin D action. The authors present two clinical cases of vitamin D dependent rickets type II, in which the alopecia was a peculiar clinical sign that allowed the diagnoses. With prolonged calcium infusions, we achieved normal seric levels of calcium and correct bone disorders; alopecia persisted. This treatment is the most effective way to control the disease.Rickets is a rare child disease especially in developed countries. Nutritional rickets remains the most prevalent condition, although congenital forms are well known. In the latest group, vitamin D dependent rickets type II is the rarest form and it can course with or without alopecia. There is a mutation on the receptor for vitamin D, with peripheral resistance to the vitamin D action. The authors present two clinical cases of vitamin D dependent rickets type II, in which the alopecia was a peculiar clinical sign that allowed the diagnoses. With prolonged calcium infusions, we achieved normal seric levels of calcium and correct bone disorders; alopecia persisted. This treatment is the most effective way to control the disease.Ordem dos Médicos2009-12-31info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1723oai:ojs.www.actamedicaportuguesa.com:article/1723Acta Médica Portuguesa; Vol. 22 No. 6 (2009): Novembro-Dezembro; 861-6Acta Médica Portuguesa; Vol. 22 N.º 6 (2009): Novembro-Dezembro; 861-61646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1723https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1723/1302Santos, RaquelNeves, SérgioGomes, ClaraNeves, FarelaCorreia, António Jorgeinfo:eu-repo/semantics/openAccess2022-12-20T10:58:43Zoai:ojs.www.actamedicaportuguesa.com:article/1723Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:17:20.667713Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Rickets vitamin-D-dependent type 2. Raquitismo vitamina D dependente tipo II. |
title |
Rickets vitamin-D-dependent type 2. |
spellingShingle |
Rickets vitamin-D-dependent type 2. Santos, Raquel |
title_short |
Rickets vitamin-D-dependent type 2. |
title_full |
Rickets vitamin-D-dependent type 2. |
title_fullStr |
Rickets vitamin-D-dependent type 2. |
title_full_unstemmed |
Rickets vitamin-D-dependent type 2. |
title_sort |
Rickets vitamin-D-dependent type 2. |
author |
Santos, Raquel |
author_facet |
Santos, Raquel Neves, Sérgio Gomes, Clara Neves, Farela Correia, António Jorge |
author_role |
author |
author2 |
Neves, Sérgio Gomes, Clara Neves, Farela Correia, António Jorge |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Santos, Raquel Neves, Sérgio Gomes, Clara Neves, Farela Correia, António Jorge |
description |
Rickets is a rare child disease especially in developed countries. Nutritional rickets remains the most prevalent condition, although congenital forms are well known. In the latest group, vitamin D dependent rickets type II is the rarest form and it can course with or without alopecia. There is a mutation on the receptor for vitamin D, with peripheral resistance to the vitamin D action. The authors present two clinical cases of vitamin D dependent rickets type II, in which the alopecia was a peculiar clinical sign that allowed the diagnoses. With prolonged calcium infusions, we achieved normal seric levels of calcium and correct bone disorders; alopecia persisted. This treatment is the most effective way to control the disease. |
publishDate |
2009 |
dc.date.none.fl_str_mv |
2009-12-31 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1723 oai:ojs.www.actamedicaportuguesa.com:article/1723 |
url |
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1723 |
identifier_str_mv |
oai:ojs.www.actamedicaportuguesa.com:article/1723 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1723 https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1723/1302 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
dc.publisher.none.fl_str_mv |
Ordem dos Médicos |
publisher.none.fl_str_mv |
Ordem dos Médicos |
dc.source.none.fl_str_mv |
Acta Médica Portuguesa; Vol. 22 No. 6 (2009): Novembro-Dezembro; 861-6 Acta Médica Portuguesa; Vol. 22 N.º 6 (2009): Novembro-Dezembro; 861-6 1646-0758 0870-399X reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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