Ring chromosome 8 syndrome
ORPHA:1450· ICD-10 Q93.2
Definition
A rare chromosomal anomaly comprising variable parts of chromosome 8. The phenotype of mosaic or non-mosaic supernumerary r(8)/mar(8) ranges from almost normal to variable degrees of minor abnormalities, and growth and mental retardation overlapping with the well-known mosaic trisomy 8 syndrome.
- Prevalence
- <1 / 1 000 000
- Age of onset
- Antenatal, Neonatal