Literature DB >> 11807893

Oculoauriculofrontonasal syndrome (OAFNS) in a nine-month-old male.

Holly A Ishmael1, Michael L Begleiter, Elizabeth J Regier, Merlin G Butler.   

Abstract

We report a nine-month-old Caucasian male with features seen in oculoauriculovertebral spectrum (OAVS) and frontonasal dysplasia sequence (FND) born to normal, non-consanguineous parents and review the literature. His malformations included a left pre-auricular skin tag, severely hypoplastic right pinna without an external canal, severely everted and hypoplastic left upper eyelid, bilateral cleft lip and palate, bifid broad nasal tip, ocular hypertelorism, micrognathia, hypoplastic mandible, an extra cervical rib on the left, hemivertebrae at T3-4, agenesis of the posterior corpus callosum with a midline lipoma, and an extra renal pelvis. This constellation of anomalies is consistent with the diagnosis of oculoauriculofrontonasal syndrome (OAFNS) which appears to be a distinct condition from either OAVS or FND but with overlapping features. Copyright 2001 Wiley-Liss, Inc.

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Year:  2002        PMID: 11807893      PMCID: PMC6715288          DOI: 10.1002/ajmg.10120

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  1 in total

1.  Neonates with extra-renal pelvis: the first 2 years.

Authors:  Ze'ev Katzir; Michaela Witzling; Gallina Nikolov; Gabriela Gvirtz; Eliana Arbel; David Kohelet; Mona Boaz; Shmuel Smetana; Mordechai Lorberboym
Journal:  Pediatr Nephrol       Date:  2005-04-19       Impact factor: 3.714

  1 in total

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