Ring chromosome 18 syndrome
ORPHA:1442· ICD-10 Q93.2
Definition
A rare autosomal anomaly characterized by variable clinical features, most commonly including hypotonia, neonatal feeding and respiratory difficulties, microcephaly, global developmental delay and intellectual disability, growth hormone deficiency, hypothyroidism, hearing loss, aural atresia, dysmorphic facial features and behavioral characteristics.
- Prevalence
- <1 / 1 000 000
- Age of onset
- Antenatal, Infancy, Neonatal