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3-метилглутаконова ацидурія, тип 4

ORPHA:67048· ICD-10 E71.1· 3-methylglutaconic aciduria type 4

Визначення(English summary)

3-methylglutaconic aciduria (3-MGA) type IV, or unclassified 3-MGA, is a clinically heterogeneous disorder characterised by increased 3-methylglutaconic acid excretion in individuals that cannot be classified as having one of the other forms of 3-MGA (3-MGA I, II or III).

Поширеність
Unknown
Успадкування
Autosomal recessive
Вік початку
Infancy, Neonatal