Oculoauriculofrontonasal syndrome

Common Name(s)

Oculoauriculofrontonasal syndrome

The OAFNS phenotype combines abnormalities of the morphogenesis of the first and second branchial arches (microtia/skin tags, epibulbar dermoids, cleft lip/palate, mandibular hypoplasia, and facial asymmetry) with malformations due to the anomalous development of the frontonasal eminence and maxillary processes (notched/bifid nasal tip, cleft lip and/or palate, and encephalocele) ({1:Gabbett et al., 2008}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Oculoauriculofrontonasal syndrome" for support, advocacy or research.

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General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Oculoauriculofrontonasal syndrome" returned 1 free, full-text research articles on human participants. First 3 results:

Early prenatal diagnosis of oculoauriculofrontonasal syndrome by three-dimensional ultrasound.
 

Author(s): J M Johnson, B Benoit, J Pierre-Louis, S Keating, D Chitayat

Journal: Ultrasound Obstet Gynecol. 2005 Feb;25(2):184-6.

 

Oculoauriculofrontonasal syndrome is a rare developmental field defect that represents an abnormal morphogenesis of the frontonasal eminence. It consists of features of both oculoauriculovertebral spectrum and frontonasal malformation. A few cases in the literature have described ...

Last Updated: 31 Dec 1969

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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

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