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Autosomal dominant Charcot-Marie-Tooth disease type 2K

ORPHA:99944DiseaseAutosomal dominantAdolescent, Adult, Childhood

Ассоциированные гены (1)

GDAP1
ganglioside induced differentiation associated protein 1
Disease-causing germline mutation(s) in
OMIM: 606598

Фенотипы (10)

Частый (30–79%)9
HP:0000762Decreased nerve conduction velocity
HP:0001288Gait disturbance
HP:0002460Distal muscle weakness
HP:0002936Distal sensory impairment
HP:0003202Skeletal muscle atrophy
HP:0003701Proximal muscle weakness
HP:0009130Hand muscle atrophy
HP:0011096Peripheral demyelination
HP:0011675Arrhythmia
Периодический (5–29%)1
HP:0001270Motor delay

Эпидемиология (2)

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

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы