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Clinical Characteristics and Long-Term Prognosis of Alport Syndrome: A Retrospective Single-Center Study

Purpose Alport syndrome (AS) is one of the most common inherited renal diseases caused due to mutations of genes encoding specific proteins of the type IV collagen family, and its major clinical manifestations include progressive renal failure, sensorineural deafness, and ocular abnormalities. We in...

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Autori principali: Hea Min Jang, Hee Sun Baek, Sun-Hee Park, Yong-Lim Kim, Chan-Duck Kim, Hee-Yeon Jung, Jang-Hee Cho, Man Hoon Han, Yong Jin Kim, Min Hyun Cho
Natura: Artigo
Lingua:Inglês
Pubblicazione: Korean Society of Pediatric Nephrology 2020-10-01
Serie:Childhood Kidney Diseases
Soggetti:
alport syndrome
end-stage renal disease
sensorineural hearing loss
Accesso online:http://www.chikd.org/upload/ckd-24-2-91.pdf
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