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A Current Landscape on Alport Syndrome Cases: Characterization, Therapy and Management Perspectives

Alport syndrome (AS) is a rare genetic disorder categorized by the progressive loss of kidney function, sensorineural hearing loss and eye abnormalities. It occurs due to mutations in three genes that encode for the alpha chains of type IV collagen. Globally, the disease is classified based on the p...

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Detalles Bibliográficos
Autores principales:	Mahrous, Nahed N., Jamous, Yahya F., Almatrafi, Ahmad M., Fallatah, Deema I., Theyab, Abdulrahman, Alanati, Bayan H., Alsagaby, Suliman A., Alenazi, Munifa K., Khan, Mohammed I., Hawsawi, Yousef M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10604007/ https://www.ncbi.nlm.nih.gov/pubmed/37893135 http://dx.doi.org/10.3390/biomedicines11102762

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