Accelerated phase of Chediak-Higashi syndrome

review of literature

Authors

DOI:

https://doi.org/10.11606/issn.1679-9836.v98i3p222-225

Keywords:

Chediak-Higashi syndrome, Lysosomes, Hypopigmentation

Abstract

Individuals affected by Chediak-Higashi syndrome present themselves clinically with several organic alterations, from mutations that affect the phagocytic and the functions of the lysosomal traffic regulator gene. The accelerated form of the syndrome presents with a series of hematological and systemic alterations, being serious and usually incurring in early death. The objective of this paper was to develop a literature review about the accelerated phase of Chediak-Higashi syndrome. The source was developed at the following databases: PubMed, The Cochrane Library, and SciELO, being included human studies published in English, Spanish or Portuguese in the last 15 years. Due to its severity, Chediak-Higashi syndrome demonstrates the importance of its knowledge by medical professionals in order to reduce the number of underdiagnostics, consequently reducing mortality rates and promoting improvement in the quality of life of the patients.

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Author Biographies

  • Lucas Soares Bezerra, Centro Universitário Maurício de Nassau - UNINASSAU

    Diretor Geral do Grupo de Pesquisa em Epidemiologia e Cardiologia (EPICARDIO) da Universidade Federal de Pernambuco, Recife, PE. Graduando em Medicina pelo Centro Universitário Maurício de Nassau, Recife, PE.

  • Marcelo Antônio Oliveira Santos-Veloso, Centro Universitário Maurício de Nassau - UNINASSAU

    Diretor Científico do Grupo de Pesquisa em Epidemiologia e Cardiologia (EPICARDIO) da Universidade Federal de Pernambuco, Recife, PE. Graduando em Medicina pelo Centro Universitário Maurício de Nassau, Recife, PE.

References

Published

2019-07-22

Issue

Section

Artigos de Revisão/Review Articles

How to Cite

Bezerra, L. S., Santos-Veloso, M. A. O., & Antunes, A. A. (2019). Accelerated phase of Chediak-Higashi syndrome: review of literature. Revista De Medicina, 98(3), 222-225. https://doi.org/10.11606/issn.1679-9836.v98i3p222-225