Alport syndrome: a genetically confirmed x-linked case with early family screening.
Introduction: Alport syndrome (AS) is a hereditary nephropathy caused by pathogenic variants in the type IV collagen genes (COL4A3, COL4A4, or COL4A5), leading to structural defects in the glomerular basement membrane, cochlea, and eye. The disease classically presents with hematuria, proteinuri...
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| Автори: | , , , , |
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| Формат: | Artigo |
| Мова: | Árabe |
| Опубліковано: |
Algerian Society of Clinical & Oncological Pharmacy
2026-06-01
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| Серія: | Batna Journal of Medical Sciences |
| Предмети: | |
| Онлайн доступ: | https://batnajms.net/wp-content/uploads/Archives/2026/06/BJMS_Kirane.pdf |
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