Opitz-Frias syndrome: Difference between revisions

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==Overview==
==Overview==
A congenital dysmorphy syndrome of characteristic facies, hypertelorism, hypospadias, dysphagia and pain during swallowing.<ref>http://ghr.nlm.nih.gov/condition/opitz-g-bbb-syndrome</ref>
Opitz-Frias syndrome is a congenital dysmorphy syndrome of characteristic facies, [[hypertelorism]], [[hypospadias]], [[dysphagia]] and [[odynophagia]] (pain during swallowing).<ref>http://ghr.nlm.nih.gov/condition/opitz-g-bbb-syndrome</ref>


==References==
==References==

Revision as of 22:54, 29 July 2012

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List of terms related to Opitz-Frias syndrome

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: Opitz G/BBB syndrome

Overview

Opitz-Frias syndrome is a congenital dysmorphy syndrome of characteristic facies, hypertelorism, hypospadias, dysphagia and odynophagia (pain during swallowing).[1]

References

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