Autosomal recessive intermediate Charcot-Marie-Tooth disease type B

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Name:
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
Description:
An extremely rare subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease characterized by a CMT neuropathy associated with developmental delay, self-abusive behavior, dysmorphic features and vestibular Schwannoma. Motor nerve conduction velocities demonstrate features of both demyelinating and axonal pathology.
ORPHAcode:
254334
Synonyms:
RI-CMT type B
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14