The case of Kennedy's bulbospinal amiotrophy: modern diagnostic opportunities
Kennedy disease is a rare neuromuscular disease associated with damage of androgen receptor gene and inherited by the X-linked recessive type. Its clinic features is characterized by a complex of neurological and extraneural disorders, including extremities peripheral paresis, bulbar syndrome. Some...
Saved in:
| Main Authors: | , , , , , , |
|---|---|
| Format: | Book |
| Published: |
LLC "MEDIAFORMAT",
2023-10-01T00:00:00Z.
|
| Subjects: | |
| Online Access: | Connect to this object online. |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|