A case of familial intracranial calcification – Fahr’s disease
Fahr’s disease, an uncommon disorder characterized by bilateral intracranial brain parenchymal calcification, presents with diverse neurological manifestations. It is often an autosomal dominantly inherited disorder with incomplete penetrance. The most frequently implicated are mutations involving S...
Saved in:
| Main Authors: | , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2025-01-01
|
| Series: | Muller Journal of Medical Sciences and Research |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/mjmsr.mjmsr_20_25 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|