Nephronophthisis
NPHP is the most common monogenic cause of CKD in children or adolescents. Extra-renal symptoms often accompany, therefore examination of retina, hearing, and skeleton is necessary in patients with CKD with insidious onset. Genes involved in NPHP-RC are mostly related in primary cilia. While genetic...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Korean Society of Pediatric Nephrology
2015-04-01
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| Edice: | Childhood Kidney Diseases |
| Témata: | |
| On-line přístup: | http://www.chikd.org/upload/ckd-19-1-23.pdf |
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