← Назад

MECP2-related severe neonatal encephalopathy

ORPHA:209370DiseaseX-linked recessiveInfancy, Neonatal

Ассоциированные гены (1)

MECP2
methyl-CpG binding protein 2
Disease-causing germline mutation(s) (loss of function) in
OMIM: 300005

Фенотипы (19)

Очень частый (80–99%)4
HP:0001298Encephalopathy
HP:0002093Respiratory insufficiency
HP:0002104Apnea
HP:0011344Severe global developmental delay
Частый (30–79%)11
HP:0000252Microcephaly
HP:0001250Seizure
HP:0001257Spasticity
HP:0001510Growth delay
HP:0002020Gastroesophageal reflux
HP:0002033Poor suck
HP:0002069Bilateral tonic-clonic seizure
HP:0004305Involuntary movements
HP:0008935Generalized neonatal hypotonia
HP:0010843EEG with focal slow activity
HP:0011471Gastrostomy tube feeding in infancy
Периодический (5–29%)4
HP:0000218High palate
HP:0002059Cerebral atrophy
HP:0002126Polymicrogyria
HP:0010841Multifocal epileptiform discharges

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