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Desminopathy

ORPHA:98909DiseaseAutosomal dominant, Autosomal recessiveAdolescent, Adult, Childhood, Infancy

Ассоциированные гены (1)

DES
desmin
Disease-causing germline mutation(s) in
OMIM: 125660

Фенотипы (18)

Очень частый (80–99%)3
HP:0003323Progressive muscle weakness
HP:0003327Axial muscle weakness
HP:0009053Distal lower limb muscle weakness
Частый (30–79%)8
HP:0001288Gait disturbance
HP:0001635Congestive heart failure
HP:0001678Atrioventricular block
HP:0002505Loss of ambulation
HP:0002747Respiratory insufficiency due to muscle weakness
HP:0005115Supraventricular arrhythmia
HP:0005157Concentric hypertrophic cardiomyopathy
HP:0030196Fatigable weakness of respiratory muscles
Периодический (5–29%)6
HP:0001645Sudden cardiac death
HP:0002522Areflexia of lower limbs
HP:0003722Neck flexor weakness
HP:0005659Thoracic kyphoscoliosis
HP:0030192Fatigable weakness of bulbar muscles
HP:0030319Weakness of facial musculature
Очень редкий (1–4%)1
HP:0003306Spinal rigidity

Эпидемиология (1)

Point prevalence
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы