A Rare Disease with Unique Findings: ROR2-associated autosomal recessive
Robinow syndrome
- Hayriye Keçeci
, - Hatice Eker,
- Hüseyin Çaksen
Hüseyin Çaksen
Necmettin Erbakan University Meram Medical Faculty Hospital
Author ProfileAbstract
Robinow syndrome is an autosomal dominant and recessive congenital
skeletal dysplasia characterized by prominent craniofacial features,
skeletal abnormalities and other anomalies. We describe the clinical
findings of a female patient who applied for dental treatment and was
diagnosed with Robinow syndrome associated with ROR2.
