Variations in expression of oral-facial-digital syndrome (type I): report of two cases.

Abstract:

:Two case reports are presented, both clearly demonstrating the diagnosis of oral-facial-digital syndrome, type I, but widely different in the expression of the condition. The first patient showed only mild expression of the syndrome. On examination at the age of 4 years there were no obvious extra oral signs, intraoral findings included the presence of supernumeraries in the primary dentition, spacing in two areas and the presence of an extra frenum. The second can be considered as a more severe case. This patient had many of the typical manifestations, including frontal bossing, a degree of zygomatic hypoplasia and clinodactyly. Orally, the most striking finding was a bilateral cleft palate which had not been diagnosed prior to examination at the age of 6 years. Other findings included multiple frena and a bifid tongue.

journal_name

Int J Paediatr Dent

authors

Driva T,Franklin D,Crawford PJ

doi

10.1111/j.1365-263x.2004.00503.x

subject

Has Abstract

pub_date

2004-01-01 00:00:00

pages

61-8

issue

1

eissn

0960-7439

issn

1365-263X

pii

503

journal_volume

14

pub_type

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