Facioscapulohumeral muscular dystrophy type 1 combined with becker muscular dystrophy: a family case report

Facioscapulohumeral muscular dystrophy type 1 combined with becker muscular dystrophy: a family case report

Facioscapulohumeral muscular dystrophy type 1 (FSHD1) and Becker muscular dystrophy (BMD) are distinct disorders caused by different genetic variations and exhibiting different inheritance patterns. The co-occurrence of both conditions within the same family is rare. In this case report, the proband...

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Bibliographic Details
Main Authors: Menglin Tan, Huiyi Huo, Jieming Feng, Chandi Wang, Suhua Jiang
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Genetics
Subjects:
FSHD1
BMD
FSHD1 combined with BMD
genetic diagnosis
case report
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2024.1522203/full
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