Infantile to late adulthood onset facioscapulohumeral dystrophy type 1: a case series
Hong Kong Med J
.
2021 Dec;27(6):444-449.
doi: 10.12809/hkmj209001.
Authors
W Y Leung
1
,
H M Luk
2
,
V Vardhanabhuti
3
,
Y Gao
4
,
K F Hui
5
,
W Y Lau
6
,
T P H Young
7
,
J T C Li
8
,
E L W Fung
9
,
A T G Chiu
1
,
I F M Lo
2
,
B H Y Chung
1
,
Y F Cheung
8
,
S H S Chan
1
Affiliations
1
Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong.
2
Clinical Genetic Service, Department of Health, Hong Kong SAR Government, Hong Kong.
3
Department of Diagnostic Radiology, The University of Hong Kong, Hong Kong.
4
Department of Medicine, Queen Mary Hospital, Hong Kong.
5
Department of Medicine and Geriatrics, United Christian Hospital, Hong Kong.
6
Department of Medicine and Geriatrics, Kwong Wah Hospital, Hong Kong.
7
Department of Medicine and Geriatrics, Ruttonjee & Tang Shiu Kin Hospitals, Hong Kong.
8
Department of Medicine, Queen Elizabeth Hospital, Hong Kong.
9
Department of Paediatrics, Prince of Wales Hospital, Hong Kong.
PMID:
34949732
DOI:
10.12809/hkmj209001
No abstract available
Publication types
Case Reports
MeSH terms
Adult
Age of Onset
Humans
Muscular Dystrophy, Facioscapulohumeral* / diagnosis
Muscular Dystrophy, Facioscapulohumeral* / genetics