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Microphthalmia-brain atrophy syndrome

ORPHA:77299Malformation syndromeAutosomal recessiveNeonatal

Фенотипы (20)

Очень частый (80–99%)2
HP:0000618Blindness
HP:0007633Bilateral microphthalmos
Частый (30–79%)11
HP:0000252Microcephaly
HP:0001257Spasticity
HP:0002013Vomiting
HP:0002376Developmental regression
HP:0002506Diffuse cerebral atrophy
HP:0006956Dilation of lateral ventricles
HP:0007162Diffuse demyelination of the cerebral white matter
HP:0007366Atrophy/Degeneration affecting the brainstem
HP:0007371Corpus callosum atrophy
HP:0030215Inappropriate crying
HP:0031165Multifocal seizures
Периодический (5–29%)7
HP:0002123Generalized myoclonic seizure
HP:0002197Generalized-onset seizure
HP:0006855Cerebellar vermis atrophy
HP:0007361Abnormality of the pons
HP:0011174Hyperkinetic seizures
HP:0031358Vegetative state
HP:0100703Tongue thrusting

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