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Amish lethal microcephaly

ORPHA:99742Malformation syndromeAutosomal recessiveAntenatal, Infancy, Neonatal

Ассоциированные гены (1)

SLC25A19
solute carrier family 25 member 19
Disease-causing germline mutation(s) in
OMIM: 606521

Фенотипы (25)

Очень частый (80–99%)11
HP:0000252Microcephaly
HP:0000340Sloping forehead
HP:0000347Micrognathia
HP:0000648Optic atrophy
HP:0000737Irritability
HP:0001320Cerebellar vermis hypoplasia
HP:0001522Death in infancy
HP:0001942Metabolic acidosis
HP:0001992Organic aciduria
HP:0011344Severe global developmental delay
HP:0011968Feeding difficulties
Частый (30–79%)8
HP:0000939Osteoporosis
HP:0001252Hypotonia
HP:0001274Agenesis of corpus callosum
HP:0001339Lissencephaly
HP:0002119Ventriculomegaly
HP:0002414Spina bifida
HP:0002509Limb hypertonia
HP:0005968Temperature instability
Периодический (5–29%)6
HP:0000185Cleft soft palate
HP:0001376Limitation of joint mobility
HP:0001558Decreased fetal movement
HP:0002069Bilateral tonic-clonic seizure
HP:0002240Hepatomegaly
HP:0004331Decreased skull ossification

Эпидемиология (2)

Prevalence at birth
>1 / 1000
Specific population
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