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Isolated lissencephaly type 1 without known genetic defects

ORPHA:1084DiseaseUnknownInfancy, Neonatal

Фенотипы (17)

Частый (30–79%)17
HP:0001250Seizure
HP:0001257Spasticity
HP:0001302Pachygyria
HP:0001319Neonatal hypotonia
HP:0002119Ventriculomegaly
HP:0002187Intellectual disability, profound
HP:0002282Gray matter heterotopia
HP:0002521Hypsarrhythmia
HP:0008936Axial hypotonia
HP:0010864Intellectual disability, severe
HP:0011201EEG with changes in voltage
HP:0011968Feeding difficulties
HP:0012469Infantile spasms
HP:0012758Neurodevelopmental delay
HP:0020219Motor seizure
HP:0031882Agyria
HP:0100952Enlarged sylvian cistern

Эпидемиология (1)

Point prevalence
Unknown
Worldwide

Лекарства и терапия

Источник: Open Targets Platform (в реальном времени)

Клинические исследования

Источник: ClinicalTrials.gov (в реальном времени)

Внешние ресурсы