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Dystonia 28

ORPHA:589618DiseaseAutosomal dominantChildhood, Infancy

Ассоциированные гены (1)

KMT2B
lysine methyltransferase 2B
Disease-causing germline mutation(s) in
OMIM: 606834

Фенотипы (27)

Очень частый (80–99%)2
HP:0007325Generalized dystonia
HP:0033049Globus pallidus hypointensity on susceptibility-weighted imaging
Частый (30–79%)8
HP:0000252Microcephaly
HP:0000473Torticollis
HP:0001249Intellectual disability
HP:0001260Dysarthria
HP:0002015Dysphagia
HP:0004322Short stature
HP:0012758Neurodevelopmental delay
HP:0031959Leg dystonia
Периодический (5–29%)15
HP:0000276Long face
HP:0000414Bulbous nose
HP:0000639Nystagmus
HP:0000716Depression
HP:0000729Autistic behavior
HP:0000739Anxiety
HP:0000821Hypothyroidism
HP:0000826Precocious puberty
HP:0001618Dysphonia
HP:0002425Anarthria
HP:0004209Clinodactyly of the 5th finger
HP:0007018Attention deficit hyperactivity disorder
HP:0007256Abnormal pyramidal sign
HP:0012048Oromandibular dystonia
HP:0031960Arm dystonia
Очень редкий (1–4%)1
HP:0000486Strabismus
Исключён (0%)1
HP:0011968Feeding difficulties

Эпидемиология (2)

Cases/families
Worldwide
Point prevalence
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы