Biemond syndrome type 2
ORPHA:141333· ICD-10 Q87.8
Definition
Biemond syndrome type 2 (BS2) is a rare genetic neurological and developmental disorder reported in a very small number of patients with a poorly defined phenotype which includes iris coloboma, short stature, obesity, hypogonadism, postaxial polydactyly, and intellectual disability. Hydrocephalus and facial dysostosis were also reported. BS2 shares features with Bardet-Biedl syndrome. There have been no further descriptions in the literature since 1997.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Unknown
- Age of onset
- Antenatal, Neonatal