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KLHL9-related early-onset distal myopathy

ORPHA:399081DiseaseAutosomal dominantAdolescent, Childhood

Ассоциированные гены (1)

KLHL9
kelch like family member 9
Disease-causing germline mutation(s) in
OMIM: 611201

Фенотипы (17)

Очень частый (80–99%)5
HP:0002936Distal sensory impairment
HP:0003458EMG: myopathic abnormalities
HP:0006466Ankle flexion contracture
HP:0009005Weakness of the intrinsic hand muscles
HP:0009063Progressive distal muscle weakness
Частый (30–79%)9
HP:0001288Gait disturbance
HP:0001430Abnormality of the calf musculature
HP:0002166Impaired vibration sensation in the lower limbs
HP:0003376Steppage gait
HP:0006844Absent patellar reflexes
HP:0006937Impaired distal tactile sensation
HP:0008954Intrinsic hand muscle atrophy
HP:0009031Amyotrophy of ankle musculature
HP:0040081Abnormal circulating creatine kinase concentration
Периодический (5–29%)1
HP:0003438Absent Achilles reflex
Очень редкий (1–4%)2
HP:0002505Loss of ambulation
HP:0003477Peripheral axonal neuropathy

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