Síndrome de Prader-Willi por deleción paterna 15q11q13 tipo 1
ORPHA:177901· ICD-10 Q87.1· Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
- Herencia
- Autosomal dominant
- Edad de inicio
- Antenatal, Neonatal
ORPHA:177901· ICD-10 Q87.1· Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1