📂 Diseases
familial multiple meningioma — Definition
Ailesel multipl menenjiyom / familial multiple meningioma
Family multipl menenjiyom is a rare disease, which can be seen in the same individual of multiple menenjiyom tumor and undergo genetic transition. It is often associated with neurofibromatosis type 2 (NF2) and is caused by NF2 gene mutations. This condition leads to the formation of benign tumors in the brain and spinal membranes (meninks) and can cause symptoms such as headaches, seizures or focal neurological defistes. The diagnosis is subject to imaging methods and genetic tests, the treatment may include surgical resection and radiotherapy.
Frequently Asked Questions
❓ What is Ailesel multipl menenjiyom?
Ailesel multipl menenjiyom; family multipl menenjiyom is a rare disease, which can be seen in the same individual of multiple menenjiyom tumor and undergo genetic transition. It is often associated with neurofibromatosis type 2 (NF2) and is caused by NF2 gene mutations. This condition leads to the formation of benign tumors in the brain and spinal membranes (meninks) and can cause symptoms such as headaches, seizures or focal neurological defistes. The diagnosis is subject to imaging methods and genetic tests, the treatment may include surgical resection and radiotherapy.
❓ What is familial multiple meningioma in Turkish?
The Turkish equivalent of "familial multiple meningioma" is Ailesel multipl menenjiyom.
❓ Which medical field is Ailesel multipl menenjiyom related to?
This term belongs to the Diseases category.