📂 الأمراض
multiple mitochondrial dysfunctions syndrome 2 — التعريف
multipl mitokondriyal disfonksiyon sendromu 2 / multiple mitochondrial dysfunctions syndrome 2
Mitokondriyal is a disease with autozomal resessive transition, caused by mutations in the NFU1 gene, which plays a role in the integration of respiratory chain complexes. It is characterized by progressive neurological degradation, metabolic acidosis, hyperglysine and pulmonary hypertension, starting in early child. The disease leads to multiple organ failure due to severe disruption in the production of mitochondrial energy and often result in early death.
الأسئلة الشائعة
❓ ما هو multipl mitokondriyal disfonksiyon sendromu 2؟
multipl mitokondriyal disfonksiyon sendromu 2; mitokondriyal is a disease with autozomal resessive transition, caused by mutations in the NFU1 gene, which plays a role in the integration of respiratory chain complexes. It is characterized by progressive neurological degradation, metabolic acidosis, hyperglysine and pulmonary hypertension, starting in early child. The disease leads to multiple organ failure due to severe disruption in the production of mitochondrial energy and often result in early death.
❓ ما معنى multiple mitochondrial dysfunctions syndrome 2 بالتركية؟
المعادل التركي لـ "multiple mitochondrial dysfunctions syndrome 2" هو multipl mitokondriyal disfonksiyon sendromu 2.
❓ ما هو المجال الطبي الذي يتعلق بـ multipl mitokondriyal disfonksiyon sendromu 2؟
هذا المصطلح ينتمي إلى فئة الأمراض.