Ictiose congênita de Arlequim: relato de um caso

Authors

DOI:

https://doi.org/10.12662/2317-3076jhbs.v7i4.2526.p432-435.2019

Keywords:

Ictiose, Ictiose de Arlequim, Anormalidades congênitas, Anormalidades da pele

Abstract

Introdução: a ictiose congênita de Arlequim é uma desordem rara constituída de herança autossômica recessiva, caracterizada pelo espessamento da pele de toda a superfície corporal. Relato do caso: apresentamos um caso de diagnóstico ecográfico pré-natal de ictiose de Arlequim, que evoluiu com óbito intrauterino. Conclusão: esse distúrbio caracteriza-se por um neonato envolto por uma membrana espessa de material córneo com fissuras generalizadas, comprometendo as funções básicas da pele e predispondo o recém-nascido a infecções e a alterações metabólicas. Com prognóstico desfavorável, o diagnóstico precoce e o tratamento de suporte visam aumentar a sobrevida e melhorar a qualidade de vida ao neonato.

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Published

2019-09-30

How to Cite

1.
Renner FW, Costa BP, Figueira FP, Ebert JP, Nascimento LS, França VT, et al. Ictiose congênita de Arlequim: relato de um caso. J Health Biol Sci. [Internet]. 2019 Sep. 30 [cited 2024 Jul. 22];7(4(Out-Dez):432-5. Available from: https://periodicos.unichristus.edu.br/jhbs/article/view/2526

Issue

Vol. 7 No. 4(Out-Dez) (2019): Journal of Health and Biological Sciences

Section

Case Report

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