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HNRNPA1-related adult-onset distal myopathy

ORPHA:399086DiseaseAdult

Ассоциированные гены (1)

HNRNPA1
heterogeneous nuclear ribonucleoprotein A1
Disease-causing germline mutation(s) in
OMIM: 164017

Фенотипы (16)

Частый (30–79%)13
HP:0001288Gait disturbance
HP:0002312Clumsiness
HP:0002936Distal sensory impairment
HP:0003376Steppage gait
HP:0003458EMG: myopathic abnormalities
HP:0003805Rimmed vacuoles
HP:0008180Mildly elevated creatine kinase
HP:0008954Intrinsic hand muscle atrophy
HP:0009005Weakness of the intrinsic hand muscles
HP:0009031Amyotrophy of ankle musculature
HP:0009063Progressive distal muscle weakness
HP:0009473Joint contracture of the hand
HP:0012548Fatty replacement of skeletal muscle
Периодический (5–29%)2
HP:0001171Split hand
HP:0009073Progressive proximal muscle weakness
Исключён (0%)1
HP:0001638Cardiomyopathy

Эпидемиология (2)

Point prevalence
<1 / 1 000 000
Worldwide
Cases/families
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы