A late-onset phenotype of familial Becker muscular dystrophy with DMD exon 26–34 deletion: a case report

Becker muscular dystrophy is a rare, progressive neuromuscular disease normally associated with an in-frame deletion in the DMD gene. Symptoms of BMD typically appear in late childhood to early adulthood, with slower progression compared to DMD. Given its initial presentation with lower limb weakness, it is challenging to distinguish BMD from other neuromuscular diseases. We report a case of a 63-year-old man who developed weakness in the pelvic girdle and both lower limbs over the past few years. After multiple unsuccessful visits to other medical facilities, the patient came to our hospital. Based on the patient’s symptoms, prior medical history, and his family members’ symptoms, we performed relevant genetic testing, which suggested that the patient has Becker muscular dystrophy associated with the DMD gene. We report a rare case of late-onset Becker muscular dystrophy associated with an in-frame deletion of exons 26–34 in the DMD gene. This case expands the phenotypic spectrum of BMD linked to this specific deletion. It highlights the importance of considering BMD in the differential diagnosis of adult patients with chronic lower-limb weakness.

Authors

Institutions

Publication Details

Journal
BMC Neurology
Published
2026-08-14
DOI
https://doi.org/10.1186/s12883-026-05287-5
Primary Topic
Muscle Physiology and Disorders
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A late-onset phenotype of familial Becker muscular dystrophy with DMD exon 26–34 deletion: a case report

Juntao Jin, Siyu Li, Rui Xin, Yingying Liu et al.
BMC Neurology
Muscle Physiology and Disorders
article

A late-onset phenotype of familial Becker muscular dystrophy with DMD exon 26–34 deletion: a case report

Juntao Jin, Siyu Li, Rui Xin, Yingying Liu, Yamin Zhang
article en

Abstract

Becker muscular dystrophy is a rare, progressive neuromuscular disease normally associated with an in-frame deletion in the DMD gene. Symptoms of BMD typically appear in late childhood to early adulthood, with slower progression compared to DMD. Given its initial presentation with lower limb weakness, it is challenging to distinguish BMD from other neuromuscular diseases. We report a case of a 63-year-old man who developed weakness in the pelvic girdle and both lower limbs over the past few years. After multiple unsuccessful visits to other medical facilities, the patient came to our hospital. Based on the patient’s symptoms, prior medical history, and his family members’ symptoms, we performed relevant genetic testing, which suggested that the patient has Becker muscular dystrophy associated with the DMD gene. We report a rare case of late-onset Becker muscular dystrophy associated with an in-frame deletion of exons 26–34 in the DMD gene. This case expands the phenotypic spectrum of BMD linked to this specific deletion. It highlights the importance of considering BMD in the differential diagnosis of adult patients with chronic lower-limb weakness.

BMC Neurology
Gansu University of Traditional Chinese Medicine (CN), Gansu Provincial Hospital (CN), First Hospital of Lanzhou University (CN), Lanzhou University (CN)
Good health and well-being
Openalex Percentile: Top 16%
Muscle Physiology and Disorders
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

A late-onset phenotype of familial Becker muscular dystrophy with DMD exon 26–34 deletion: a case report — Juntao Jin, Siyu Li, et al. · BMC Neurology (2026) | TGRS Research Map | TGRS