Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients.
Feng LinKang YangXin LinMing JinLong ChenFu-Ze ZhengLiang-Liang QiuZhi-Xian YeHai-Zhu ChenMin-Ting LinNing WangZhi-Qiang WangPublished in: Orphanet journal of rare diseases (2023)
We determined the prevalence of different LGMD subtypes in Southeast China, described the detailed clinical manifestations and distinct muscle MRI patterns of these LGMD subtypes and reported the frequent mutations and the cardiorespiratory involvement frequency in our cohort, all of which might facilitate the differential diagnosis of LGMDs, allowing more timely treatment and guiding future clinical trials.
Keyphrases
- clinical trial
- high resolution
- magnetic resonance imaging
- risk factors
- skeletal muscle
- contrast enhanced
- electronic health record
- body composition
- big data
- randomized controlled trial
- magnetic resonance
- combination therapy
- machine learning
- single molecule
- diffusion weighted imaging
- study protocol
- fluorescence imaging
- replacement therapy
- open label