📂 Diseases
peroxisomal disease — Definition
Peroksizomal hastalık / peroxisomal disease
Peroxizomal diseases are genetic metabolic diseases caused by structural or functional disorders of the peroklessoma organs in cells. These diseases lead to disruptions in peroxizomal functions such as oxidation, plasmalogen synthesis and detoxification of reactive oxygen species. Clinical findings include neurological recovery, vision and hearing loss, skeleton abnormalities and liver dysfunction. Zellweger syndrome is the main examples of neonatal adrenolökodistrophy and infantile Refsum disease in this group.
Frequently Asked Questions
❓ What is Peroksizomal hastalık?
Peroksizomal hastalık; peroxizomal diseases are genetic metabolic diseases caused by structural or functional disorders of the peroklessoma organs in cells. These diseases lead to disruptions in peroxizomal functions such as oxidation, plasmalogen synthesis and detoxification of reactive oxygen species. Clinical findings include neurological recovery, vision and hearing loss, skeleton abnormalities and liver dysfunction. Zellweger syndrome is the main examples of neonatal adrenolökodistrophy and infantile Refsum disease in this group.
❓ What is peroxisomal disease in Turkish?
The Turkish equivalent of "peroxisomal disease" is Peroksizomal hastalık.
❓ Which medical field is Peroksizomal hastalık related to?
This term belongs to the Diseases category.