Oculoauricular syndrome
| Oculoauricular syndrome | |
|---|---|
| Oculoauricular syndrome is inherited in an autosomal recessive manner. | |
| Specialty | Medical genetics |
Oculoauricular syndrome is a rare genetic condition affecting the eyes and ears. It is due to mutations in the H6 family homeobox 1 (HMX1) gene. It is also known as the Schorderet-Munier-Franceschetti syndrome.