Lisencefalie, typ 1, způsobená mutací genu pro doublekortin
ORPHA:2148· ICD-10 Q04.3· Lissencephaly type 1 due to doublecortin gene mutation
- Prevalence
- Unknown
- Dědičnost
- X-linked recessive
- Věk nástupu
- Adolescent, Childhood, Infancy, Neonatal
ORPHA:2148· ICD-10 Q04.3· Lissencephaly type 1 due to doublecortin gene mutation