Skip to content
Open access

A Case Report of a Novel Myelin Protein Zero (MPZ) Pathogenic Variant in Charcot–Marie–Tooth Disease Combined With Type 2 Diabetes

Jan 2026 · Case Reports in Genetics · Vol 2026 · 0 citations · 33 references
Medicine

TL;DR

A patient with an intermediate CMT (CMT‐Int) type carrying a novel pathogenic variant in the MPZ gene combined with type 2 diabetes developed type 2 diabetes following pancreatic cyst surgery in September 2022, and Electrophysiological findings suggested widespread peripheral nerve damage affecting both sensory and motor fibers.

Abstract

Charcot–Marie–Tooth (CMT) disease is the collective term for the most common inherited peripheral neuropathies, affecting both motor and sensory nerves. A typical CMT patient presents with slowly progressive distal muscle weakness and atrophy that primarily involves the small foot muscles, peroneal muscles, and, often later, the muscles of the hands and forearms. Foot deformities, most commonly pes cavus and claw toes, are common and can lead to gait impairments. In this paper, we report a patient with an intermediate CMT (CMT‐Int) type carrying a novel pathogenic variant in the MPZ gene combined with type 2 diabetes. The patient’s initial symptoms included a gradual onset of muscle wasting, weakness, and sensory impairment in the lower limbs. Electrophysiological findings suggested widespread peripheral nerve damage affecting both sensory and motor fibers, with a predominant demyelinating pattern accompanied by axonal damage. Genetic testing identified a previously unreported heterozygous mutation in the MPZ gene, specifically c.548G > A, p.Trp183∗. This alteration results in the replacement of the 183rd amino acid (tryptophan) by a stop codon. This premature stop codon is predicted to escape nonsense‐mediated mRNA decay, resulting in a C‐terminally truncated protein that may exert a dominant‐negative effect. Although a different variant affecting the same codon (c.549G > A, p.Trp183∗, VCV000917145.1) has been documented, this particular pathogenic mutation has not been previously recorded. After being diagnosed with CMT, the patient developed type 2 diabetes following pancreatic cyst surgery in September 2022. The presence of both conditions exposed her peripheral nerves to congenital structural abnormalities combined with the metabolic consequences of chronic hyperglycemia and local ischemia, thereby exacerbating nerve injury.

Read PDF

Similar papers

Oct 2026

AUTOSOMAL RECESSIVE AXONAL NEUROPATHY WITH NEUROMYOTONIA CAUSED BY A MUTATION IN THE HINT1 GENE: A REPORT OF TWO CLINICAL CASES

Hereditary sensorimotor neuropathies are characterized by high genetic heterogeneity, which complicates their diagnosis. Autosomal recessive axonal neuropathy with neuromyotonia (ARAN-NM), associated with mutations in the HINT1 gene, is a rare but clinically recognizable disease. Description of clinical cases is import...

I. Komarova, V. Zykov, A. S. Rubtsova et al. · 0 citations
Open access Sep 2026

Case Report: Bilateral pes planovalgus: an uncommon pediatric orthopedic presentation of Charcot–Marie–Tooth disease type 4B1

Charcot–Marie–Tooth (CMT) disease is an inherited motor and sensory neuropathy that typically presents with cavovarus foot deformity. Pes planovalgus is uncommon in CMT and, while noted incidentally in multicenter cohort studies of CMT4B subtypes, has not been described as the predominant orthopedic manifestation in a...

H. Alkhunayfir, Rahaf Alrasheed, Abdelhamid Elshahid Hassan et al. · 0 citations
Open access Sep 2026

Genetic basis of Charcot-Marie-Tooth disease in Pakistani consanguineous families

Charcot-Marie-Tooth (CMT) is a group of inherited neuromuscular disorders with diverse clinical features such as muscle weakness and atrophy of the distal regions, foot deformities, sensory loss and decreased or absent reflexes. With the diverse inheritance patterns including dominant, recessive, and X-linked, it exhib...

Zafar Ali, M. Jameel, J. Klar et al. · 0 citations
Open access Sep 2026

Inclusion-Body Myopathy with Paget Disease of the Bone and Frontotemporal Dementia (IBMPFD) with SCN4A Mutation: Modifying Factor or Not?

A 56-year-old man with a family history of myopathy developed generalized muscle weakness at age 45. At age 52, he was diagnosed with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia (IBMPFD), confirmed by muscle pathology and a pathogenic VCP mutation (c.464G>A, p.R155H). Concurrent testi...

Sekai Tsujimoto, Koji Hayashi, Mamiko Sato et al. · 0 citations
Open access Sep 2026

A wolf in sheep’s clothing: myositis mimicking motor neuron disease – a case report

Idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of immune-mediated muscle disorders typically presenting with proximal muscle weakness and elevated creatine kinase levels. Atypical presentations, particularly in elderly individuals, may mimic motor neuron disease (MND), creating significant diagnost...

Thamil Pavai, Juhin P. P., M. K. et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.