oculodentodigital

oc·u·lo·den·to·dig·i·tal

(ok'yū-lō-den'tō-dij'i-tăl),

Relating to the eyes, teeth, and fingers.

oc·u·lo·den·to·dig·i·tal

(ok'yū-lō-den'tō-dij'i-tăl)

Relating to eyes, teeth, and fingers.

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References in periodicals archive ?

Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia.

No evidence for clinical utility in investigating the connexin genes GJB2, GJB6 and GJA1 in non-syndromic hearing loss in black Africans

But it should be kept in mind that microphthalmia, which is one of the most common feature in many syndromes can also be observed in Micro syndrome (4), oculodentodigital dysplasia (5,6) (ODDD), oculofaciocardiodental syndrome (7) (OFCDS), and Lenz microphthalmia syndrome (1-3).

Oculodentodigital dysplasia (ODDD) is a rare autosomal dominant inherited disorder affecting the development of the face, eyes, teeth, and limbs.

A case with microphthalmia and multiple congenital anomalies/mikroftalmi ve coklu konjenital anomalili bir olgu