Autosomal recessive Charcot-Marie-Tooth disease with hoarseness

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Autosomal recessive Charcot-Marie-Tooth disease with hoarseness

Synonyms: ARCMT2K | Autosomal recessive axonal CMT4C4 | Autosomal recessive axonal Charcot-Marie-Tooth disease type 2K

A severe early-onset form of axonal CMT peripheral sensorimotor polyneuropathy.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version March 2024

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Autosomal recessive Charcot-Marie-Tooth disease with hoarseness?

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Advocacy Organizations

Hereditary Neuropathy Foundation

Hereditary Neuropathy Foundation (HNF) is a non-profit 501(c)3 organization which mission is to increase awareness and accurate diagnosis of Charcot-Marie-Tooth (CMT) and related inherited neuropathies, support patients and families with critical information to improve quality of life, and fund research that will lead to treatments and cures.

Clinical Trials

For a list of clinical trials in this disease area, please click here.