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Features include: Hyporeflexia, Axonal degeneration/regeneration, Skeletal muscle atrophy, and Peripheral axonal neuropathy and 6 more.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Brain and nerves | 3 | Hyporeflexia, Peripheral axonal neuropathy, Steppage gait |
No clinical trials have been registered for Charcot-Marie-Tooth disease, dominant intermediate A.
8 publications have been identified in PubMed for Charcot-Marie-Tooth disease, dominant intermediate A. Research spans Basic Science / Preclinical (50%), Other (13%), and Review / Meta-Analysis (13%).
Kavoosi S (2025). [PMID: 41357705](https://pubmed.ncbi.nlm.nih.gov/41357705/). *Iran J Public Health*. [Review / Meta-Analysis]
Spontarelli Fruit K (2025). [PMID: 41048924](https://pubmed.ncbi.nlm.nih.gov/41048924/). *Neurol Genet*. [Basic Science / Preclinical]
Pérez-López DO (2025). [PMID: 39975190](https://pubmed.ncbi.nlm.nih.gov/39975190/). *bioRxiv*. [Basic Science / Preclinical]
Cakar A (2025). [PMID: 39776111](https://pubmed.ncbi.nlm.nih.gov/39776111/). *Eur J Neurol*. [Epidemiology / Natural History]
Pérez-López DO (2025). [PMID: 40635134](https://pubmed.ncbi.nlm.nih.gov/40635134/). *Hum Mol Genet*. [Basic Science / Preclinical]
Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 3:00 PM UTC
Online Mendelian Inheritance in Man
Common questions about Charcot-Marie-Tooth disease, dominant intermediate A
2 |
Skeletal muscle atrophy, Limb muscle weakness |
Bones and joints | 1 | Skeletal muscle atrophy |
Arms and legs | 1 | Limb muscle weakness |
Unknown (2024). [PMID: 38668692](https://pubmed.ncbi.nlm.nih.gov/38668692/). *Hum Mol Genet*. [Other]
Cabello-Murgui J (2024). [PMID: 39287469](https://pubmed.ncbi.nlm.nih.gov/39287469/). *Eur J Neurol*. [Case Report / Case Series]