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...
محفوظ في:
| المؤلفون الرئيسيون: | , , , , , , , , , |
|---|---|
| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Korean Society of Pediatric Nephrology
2020-10-01
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| سلاسل: | Childhood Kidney Diseases |
| الموضوعات: | |
| الوصول للمادة أونلاين: | http://www.chikd.org/upload/ckd-24-2-91.pdf |
| الوسوم: |
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