Lysosomal Storage Diseases

Alroy, Joseph; Lyons, Jeremiah A.

Alroy, Joseph; Lyons, Jeremiah A..

Alroy, Joseph; Tufts University School of Medicine1. Department of Pathology. Boston. US
Lyons, Jeremiah A.; Tufts University. Cummings School of Veterinary Medicine. Department of Biomedical Sciences. North Grafton. US

J. inborn errors metab. screen ; 2: e130001, 2014. tab, graf

Artículo en Inglés | LILACS-Express | LILACS | ID: biblio-1090853

ABSTRACT

ABSTRACT

Abstract Lysosomal storage diseases are a group of inherited and acquired disorders. They are characterized by interruption of recycling of cellular and extracellular molecules. Clinically, they are presented as developmental and neurological symptoms similar to other inherited and acquired disorders. This article reviews the function of lysosomes, the current mechanisms that cause the interruption of recycling, the consequences that are manifested clinically, and the methods to diagnose these disorders.

Clinical manifestations; Diagnostic tools; Lysosome function

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Texto completo: Disponible Índice: LILACS (Américas) Idioma: Inglés Revista: J. inborn errors metab. screen Asunto de la revista: Medicina Cl¡nica / Patologia Año: 2014 Tipo del documento: Artículo País de afiliación: Estados Unidos Institución/País de afiliación: Tufts University School of Medicine1/US / Tufts University/US

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