Marfan Sindromi
fbn1 genemyopiahypermobile jointsmitral valve prolapselens dislocation
54 betPPTX47 ko'rildi0 marta sotilgan
8 000 so'm
Sotuvchi Medic😎227 ta hujjat sotilgan
Tavsif
Marfan syndrome is an autosomal-dominant genetic disorder caused by a mutation in the FBN1 gene, affecting the skeletal, ocular, and cardiovascular systems. Characterized by aortic root dilation, lens dislocation, and unique body structure. Early diagnosis is crucial to prevent aortic dissection
Hujjat haqida
- Kategoriya
- Taqdimotlar | Tibbiyot
- Format
- PPTX
- Hajmi
- 54 bet
- Fayl hajmi
- 35.59 MB
- Muallif
- Sotuvchi Medic😎
- Qo'shilgan
- 24.03.2026
