Orofacial Manifestations of Autosomal Recessive Robinow's Syndrome: A Rare Case Report.

Autor: MALI, SANTOSH, BANSAL, NEHA, DHOKAR, AMOL, YADAV, MONICA
Předmět:
Zdroj: Journal of Clinical & Diagnostic Research; Mar2016, Vol. 10 Issue 3, p9-10, 2p
Abstrakt: Robinow's syndrome is a very rare genetic disorder which bears a resemblance to a foetal face. It is characterized by short-limbed dwarfism, defects in vertebral segmentation and abnormalities in the head, face and external genitalia. It has a genetic heterogeneity with autosomal dominant and recessive forms which relates to the severity of phenotype presentation. A rare case of an autosomal recessive form of Robinow's syndrome is presented with emphasis on, characteristic craniofacial and intraoral manifestations to aid in diagnosis and dental management of this patient. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index