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Malonic aciduria

ORPHA:943DiseaseAutosomal recessiveChildhood

Ассоциированные гены (1)

MLYCD
malonyl-CoA decarboxylase
Disease-causing germline mutation(s) in
OMIM: 606761

Фенотипы (19)

Очень частый (80–99%)4
HP:0000750Delayed speech and language development
HP:0001332Dystonia
HP:0012120Methylmalonic aciduria
HP:0034657Elevated urine malonic acid level
Частый (30–79%)10
HP:0000252Microcephaly
HP:0001250Seizure
HP:0001263Global developmental delay
HP:0001508Failure to thrive
HP:0001510Growth delay
HP:0001638Cardiomyopathy
HP:0001942Metabolic acidosis
HP:0001943Hypoglycemia
HP:0011968Feeding difficulties
HP:6000355Reduced malonyl-CoA decarboxylase activity in cultured fibroblasts
Периодический (5–29%)5
HP:0001252Hypotonia
HP:0001254Lethargy
HP:0001946Ketosis
HP:0002013Vomiting
HP:0002014Diarrhea

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