Academic Journal

An overview of molecular mechanisms in fabry disease

التفاصيل البيبلوغرافية
العنوان: An overview of molecular mechanisms in fabry disease
المؤلفون: Amodio, Federica, Caiazza, Martina, Monda, Emanuele, Rubino, Marta, Capodicasa, Laura, Chiosi, Flavia, Simonelli, Vincenzo, Dongiglio, Francesca, Fimiani, Fabio, Pepe, Nicola, Chimenti, Cristina, Calabrò, Paolo, Limongelli, Giuseppe
المساهمون: Amodio, Federica, Caiazza, Martina, Monda, Emanuele, Rubino, Marta, Capodicasa, Laura, Chiosi, Flavia, Simonelli, Vincenzo, Dongiglio, Francesca, Fimiani, Fabio, Pepe, Nicola, Chimenti, Cristina, Calabrò, Paolo, Limongelli, Giuseppe
بيانات النشر: MDPI
Basel, Switzerland
سنة النشر: 2022
المجموعة: Sapienza Università di Roma: CINECA IRIS
مصطلحات موضوعية: fabry disease, GLA gene, biomarker, mutation, α-galactosidase A
الوصف: Fabry disease (FD) (OMIM #301500) is a rare genetic lysosomal storage disorder (LSD). LSDs are characterized by inappropriate lipid accumulation in lysosomes due to specific enzyme deficiencies. In FD, the defective enzyme is alpha-galactosidase A (alpha-Gal A), which is due to a mutation in the GLA gene on the X chromosome. The enzyme deficiency leads to a continuous deposition of neutral glycosphingolipids (globotriaosylceramide) in the lysosomes of numerous tissues and organs, including endothelial cells, smooth muscle cells, corneal epithelial cells, renal glomeruli and tubules, cardiac muscle and ganglion cells of the nervous system. This condition leads to progressive organ failure and premature death. The increasing understanding of FD, and LSD in general, has led in recent years to the introduction of enzyme replacement therapy (ERT), which aims to slow, if not halt, the progression of the metabolic disorder. In this review, we provide an overview of the main features of FD, focusing on its molecular mechanism and the role of biomarkers.
نوع الوثيقة: article in journal/newspaper
اللغة: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/36291669; info:eu-repo/semantics/altIdentifier/wos/WOS:000872334500001; volume:12; issue:10; numberofpages:15; journal:BIOMOLECULES; https://hdl.handle.net/11573/1681150; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85140430915
DOI: 10.3390/biom12101460
الاتاحة: https://hdl.handle.net/11573/1681150
https://doi.org/10.3390/biom12101460
Rights: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.E0AC92EB
قاعدة البيانات: BASE