Charcot-Marie-Tooth disease type 2E
Charcot-Marie-Tooth disease type 2E
Definition
Autosomal dominant Charcot-Marie-Tooth disease type 2E (CMT2E) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2E onset is in the first to 6th decade with a gait anomaly and a leg weakness that reaches the arms secondarily. Tendon reflexes are reduced or absent and, after years, all patients have a pes cavus. Other signs may be present, including hearing loss and postural tremor.
Also known as autosomal dominant Charcot-Marie-Tooth disease type 2E, Charcot-Marie-Tooth disease type 2 caused by mutation in NEFL, Charcot-Marie-Tooth disease, type 2E, CMT2E, NEFL Charcot-Marie-Tooth disease type 2 — per MONDO
Also identified as
- DOID 0110165 per MONDO
- MESH C537994 per MONDO
- NCIT C134953 per MONDO
- OMIM 607684 per MONDO
- Orphanet 99939 per MONDO
- SCTID 717012004 per MONDO
- UMLS C1843225 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Musculature | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Musculature | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Musculoskeletal system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Musculoskeletal system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Nervous system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Nervous system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Peripheral nervous system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Peripheral nervous system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |