Alegría CFG, Cárdenas MMA, Montoya CMR

Language: Spanish
References: 8
Page: 100-103
PDF size: 387.65 Kb.

ABSTRACT

Oculo-dento-digital syndrome is a malformation that affects: face, hair, eyes, dental organs, fingers and bones, is usually inherited in an autosomal dominant pattern, but sporadic and autosomal recessive cases have also been identified. They report around 300 isolated cases, with an incidence of one per 10 million. We present a case of a 10-year-old female who presents 23% of the characteristics of ODD dysplasia, with new findings for this syndrome such as: coloboma, polydactyly on the right foot, bilateral hallux valgus, dyslexia and dysgraphia. A clinical genetic evaluation helps to identify it at a young age, and to recognize the alterations that may require medical therapy, the treatment in patients carrying the ODD syndrome requires the integration of a multidisciplinary health team in order to provide well-being to the patient.

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