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Alport Sendromu

Alport Sendromu

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<strong>Alport</strong> <strong>Sendromu</strong><br />

Klinik<br />

• Herediter,<br />

progresif,hematürik<br />

• Klasik — X’e bağlı<br />

• Nadiren otozomal resesif<br />

ve dominant formlar<br />

• Hematüri, progresif<br />

böbrek yetmezliği<br />

• Oküler defektler, işitme<br />

kaybı<br />

Patogenez<br />

• Klasik form — COL4A5<br />

mutasyonu<br />

• Nadir formlar —<br />

COL4A3 veya COL4A4<br />

mutasyonu<br />

• Defektif type IV<br />

kollajen birikimi

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