A case report on autosomal recessive Robinow syndrome.

Abstract:

BACKGROUND:Robinow syndrome or "foetal face" syndrome is an extremely rare genetic disorder with characteristic skeletal and orofacial findings. The purpose of the present case report is to describe the clinical findings of an 8 year-old female patient with autosomal recessive Robinow syndrome. CASE REPORT:The patient was born to consanguineous parents and had anomalies typical of the recessive type of the syndrome such as short stature, mesomelic limb shortening, vertebral anomalies and dysmorphic facial features. Besides typical orodental findings, she also had root malformation in mandibular incisors, which is unusual finding of recessive type of Robinow syndrome. This case report emphasizes the importance of oral and dental manifestations of this syndrome.

journal_name

Eur J Paediatr Dent

authors

Eronat N,Cogulu D,Ozkinay F

subject

Has Abstract

pub_date

2009-09-01 00:00:00

pages

147-50

issue

3

eissn

1591-996X

issn

2035-648X

journal_volume

10

pub_type

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