Abstract The 2020 Kidney Disease: Improving Global Outcomes (KDIGO) Clinical Practice
Guideline on the Evaluation and Management of Candidates for Kidney Transplantation is …

Rationale & Objective There is limited information about the association between primary
kidney disease and donor relatedness with transplant outcomes. This study addresses this …

Alport syndrome is a hereditary glomerular basement membrane disease caused by
mutations in the COL4A3/4/5 genes encoding the type IV collagen alpha 3–5 chains. Most …

Background Mutations in COL4A5 are responsible for 80% of cases of X-linked Alport
Syndrome (XLAS). Although genes that cause AS are well characterized, people with AS …

Background Historically, due to the lack of distinct clinical symptoms, Alport syndrome, a
hereditary kidney disease prevalent in children and a leading cause of kidney failure, has …

Alport 综合征(AS) 是我国常见的具有遗传异质性的儿童肾脏疾病, 以血尿, 听力损坏,
眼部病变及进行性肾功能衰竭等为临床特点, 又被称为家族性出血性肾炎, 遗传性进行性肾炎 …

Alport syndrome is a genetic kidney disease that causes worsening of kidney function over
time, often progressing to kidney failure. Some types of Alport syndrome cause other …

Hearing impairment is an immensely diagnosed genetic cause, 5% of the total world
population effects with different kind of congenital hearing loss (HL). In third-world countries …

Hereditary nephritis usually refers to Alport syndrome and thin basement membrane
nephropathy. Hematuria occurs in about 6% of the pediatric population and is mainly …

Alport syndrome (AS) is a hereditary disease that is characterized by progressive kidney
disease, sensorineural hearing loss, and ocular lesions. 1 The responsible genes for AS are …