A novel NDRG1 mutation in a non‐Romani patient with CMT4D/HMSN‐Lom. Issue 1 (March 2017)

• Record Type: Journal Article
• Authors: Piscosquito, Giuseppe; Magri, Stefania; Saveri, Paola; Milani, Micaela; Ciano, Claudia; Farina, Laura; Taroni, Franco; Pareyson, Davide
• Is Part Of: Journal of the peripheral nervous system. Volume 22:Issue 1(2017)
• Page Start: 47
• Page End: 50
• Publication Date: 2017-03
• Subjects: Charcot‐Marie‐Tooth disease -- CMT4 -- demyelinating recessive CMT -- hereditary motor and sensory neuropathy Lom type -- N‐Myc downstream‐regulated gene 1 (NDRG1); Nervous system -- Periodicals; Nerves, Peripheral -- Diseases -- Periodicals; Peripheral Nervous System Diseases -- Periodicals; Peripheral Nervous System -- Periodicals; 612.81
• DOI: 10.1111/jns.12201
• Languages: English
• ISSNs: 1085-9489

Abstract

Abstract: Charcot‐Marie‐Tooth disease type 4D (CMT4D), also known as hereditary motor and sensory neuropathy Lom type (HMSNL), is an autosomal recessive, early onset, severe demyelinating neuropathy with hearing loss, caused by N‐Myc downstream‐regulated gene 1 ( NDRG1 ) mutations. CMT4D is rare with only three known mutations, one of which (p.Arg148Ter) is found in patients of Romani ancestry and accounts for the vast majority of cases. We report a 38‐year‐old Italian female with motor development delay, progressive neuropathy, and sensorineural deafness. Magnetic resonance imaging showed slight atrophy of cerebellum, medulla oblongata, and upper cervical spinal cord. She had a novel homozygous NDRG1 frameshift mutation (c.739delC; p.His247ThrfsTer74). The identification of this NDRG1 mutation confirms that CMT4D is not a private Romani disease and should be considered in the differential diagnosis of recessive demyelinating CMT.