Opitz-Frias syndrome: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
(One intermediate revision by the same user not shown) | |||
Line 6: | Line 6: | ||
==Overview== | ==Overview== | ||
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== |
Latest revision as of 22:54, 29 July 2012
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]