Demyelinizace mozku způsobená deficitem methionin adenosyltransferázy
ORPHA:168598· ICD-10 E72.1· Methionine adenosyltransferase I/III deficiency
- Prevalence
- <1 / 1 000 000
- Dědičnost
- Autosomal recessive
- Věk nástupu
- Infancy
ORPHA:168598· ICD-10 E72.1· Methionine adenosyltransferase I/III deficiency