← Назад

Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3

ORPHA:62DiseaseAutosomal recessiveAdolescent, Childhood

Ассоциированные гены (1)

SGCA
sarcoglycan alpha
Disease-causing germline mutation(s) in
OMIM: 600119

Фенотипы (14)

Частый (30–79%)13
HP:0001771Achilles tendon contracture
HP:0002359Frequent falls
HP:0002515Waddling gait
HP:0003236Elevated circulating creatine kinase concentration
HP:0003307Hyperlordosis
HP:0003391Gowers sign
HP:0003551Difficulty climbing stairs
HP:0003560Muscular dystrophy
HP:0003691Scapular winging
HP:0003701Proximal muscle weakness
HP:0003707Calf muscle pseudohypertrophy
HP:0006467Limited shoulder movement
HP:0030051Tip-toe gait
Периодический (5–29%)1
HP:0002943Thoracic scoliosis

Эпидемиология (2)

Point prevalence
<1 / 1 000 000
United Kingdom
Point prevalence
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы