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Megalencephalic leukoencephalopathy with subcortical cysts

ORPHA:2478DiseaseAutosomal dominant, Autosomal recessiveInfancy, Neonatal

Ассоциированные гены (2)

MLC1
modulator of VRAC current 1
Disease-causing germline mutation(s) in
OMIM: 605908
HEPACAM
hepatic and glial cell adhesion molecule
Disease-causing germline mutation(s) in
OMIM: 611642

Фенотипы (18)

Частый (30–79%)10
HP:0000708Atypical behavior
HP:0001250Seizure
HP:0001251Ataxia
HP:0001257Spasticity
HP:0001268Mental deterioration
HP:0002317Unsteady gait
HP:0002333Motor deterioration
HP:0005490Postnatal macrocephaly
HP:0007341Diffuse swelling of cerebral white matter
HP:6000461Cerebral subcortical cyst
Периодический (5–29%)8
HP:0000717Autism
HP:0001249Intellectual disability
HP:0001332Dystonia
HP:0002071Abnormality of extrapyramidal motor function
HP:0002133Status epilepticus
HP:0002305Athetosis
HP:0002312Clumsiness
HP:0012762Cerebral white matter atrophy

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