-
classification of
LGMDs in 1995. The
classification scheme at that time
denoted autosomal dominant LGMDs as 'LGMD1' and
autosomal recessive LGMDs as 'LGMD2.'...
-
deficiency (osteomalic myopathy).
Although limb-girdle
muscular dystrophies (
LGMDs)
involve fixed muscle weakness, LGMDR8 also
involves muscle fatigue; as...
-
affected protein.
LGMD D1 DNAJB6-related
LGMD D2 TNP03-related
LGMD D3 HNRNPDL-related
LGMD D4 calpain3-related
LGMD D5
collagen 6-related
LGMD R1 calpain3-related...
- most
common type of
autosomal recessive limb-girdle
muscular dystrophy (
LGMD). It
preferentially affects the
muscles of the hip
girdle and
shoulder girdle...
- (DMD) and
Becker muscular dystrophy (BMD)
Myotonic dystrophy Limb-Girdle (
LGMD)
Facioscapulohumeral dystrophy (FSHD)
Congenital dystrophy (CMD)
Distal (DD)...
- neck and
shoulder girdle muscles.
LGMD R28 has calf
hypertrophy and exercise-induced
muscle fatigue and pain.
LGMD R8 has calf
pseudohypertrophy and exercise-induced...
- calpain3-related (formerly
LGMD 2A), LGMDR2 dysferlin-related (
LGMD 2B), LGMDR3 α-sarcoglycan-related (
LGMD 2D), LGMDR5 γ-sarcoglycan-related (
LGMD 2C), and LGMDR6...
-
muscular dystrophy might have mild
cerebellar hypoplasia in some
cases . CMD/
LGMD without MR-first
years of a
newborn begins with weakness,
which affects motive...
-
Sarcoglycanopathies are
autosomal recessive limb
girdle muscular dystrophies (
LGMDs)
caused by
mutations in any of the four
sarcoglycan genes: α (LGMD2D), β...
- PMC 2987336. PMID 20068593. Straub, Volker; Murphy, Alexander; Udd, Bjarne;
LGMD workshop study group (August 2018). "229th ENMC
international workshop: Limb...
