Autosomal dominant slowed nerve conduction velocity

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Autosomal dominant slowed nerve conduction velocity

A rare hereditary demyelinating motor and sensory neuropathy characterized by slowed nerve conduction velocities in the absence of clinically apparent neurological deficits gait abnormalities or muscular atrophy associated with a germline mutation in the ARGHEF10 gene.

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 dominant slowed nerve conduction velocity?

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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.