Charcot‐Marie‐Tooth disease in children
Abstract Charcot‐Marie‐Tooth (CMT) disease represents a diverse group of inherited neuropathies with a broad spectrum of symptoms. It is the most prevalent inherited neuropathy, with an estimated prevalence ranging from 9.7 to 82 cases per 100,000 individuals. Despite this, CMT comprises only 118 of...
Saved in:
| Main Authors: | Ezgi Saylam, Praveen Kumar Ramani, Ruthwik Duvuru, Brett Haley, Aravindhan Veerapandiyan |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wiley
2024-12-01
|
| Series: | Annals of the Child Neurology Society |
| Subjects: | |
| Online Access: | https://doi.org/10.1002/cns3.20093 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Genetically confirmed Charcot–Marie–Tooth disease type 2A manifesting with postural tremor: a case report
by: Salhadin Mohammed, et al.
Published: (2024-11-01) -
Wellbeing measurement among adults with Charcot-Marie-Tooth disease
by: Payton D. Rule, et al.
Published: (2024-01-01) -
Hereditary sensory autonomic neuropathy type VI in the age of genetic testing
by: Lekshmi Peringassery Sateesh, et al.
Published: (2024-12-01) -
Hereditary neuropathy with liability to pressure palsies: a case series report
by: S. Naudžiūnaitė, et al.
Published: (2020-12-01) -
Diagnostic dilemma: Leber's hereditary optic neuropathy in a 70-year-Old woman
by: Alexandra Pietraszkiewicz, et al.
Published: (2024-12-01)