← Назад

Dystonia-parkinsonism-hypermanganesemia syndrome

ORPHA:521406DiseaseAutosomal recessiveInfancy

Ассоциированные гены (1)

SLC39A14
solute carrier family 39 member 14
Disease-causing germline mutation(s) in
OMIM: 608736

Фенотипы (26)

Частый (30–79%)26
HP:0000253Progressive microcephaly
HP:0000338Hypomimic face
HP:0001249Intellectual disability
HP:0001257Spasticity
HP:0001263Global developmental delay
HP:0001272Cerebellar atrophy
HP:0001300Parkinsonism
HP:0001332Dystonia
HP:0001337Tremor
HP:0001347Hyperreflexia
HP:0002059Cerebral atrophy
HP:0002067Bradykinesia
HP:0002376Developmental regression
HP:0002465Poor speech
HP:0002483Bulbar signs
HP:0002505Loss of ambulation
HP:0002650Scoliosis
HP:0002828Multiple joint contractures
HP:0003487Babinski sign
HP:0008936Axial hypotonia
HP:0011448Ankle clonus
HP:0012048Oromandibular dystonia
HP:0012407Scissor gait
HP:0030890Hyperintensity of cerebral white matter on MRI
HP:0032097Hypermanganesemia
HP:0100660Dyskinesia

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