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Hayriye Keçeci
Hayriye Keçeci

Public Documents 1
A Rare Disease with Unique Findings: ROR2-associated autosomal recessive Robinow synd...
Hayriye Keçeci
Hatice Eker

Hayriye Keçeci

and 2 more

April 13, 2022
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.

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