Literature DB >> 4025404

Apert syndrome with frontonasal encephalocele.

J R Waterson, M A DiPietro, M Barr.   

Abstract

We describe a female infant with Apert syndrome (acrocephalosyndactyly, type I) and a frontonasal encephalocele with unremarkable family history.

Entities:  

Mesh：

Year:  1985        PMID： 4025404     DOI： 10.1002/ajmg.1320210422

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


  3 in total

1.  Apert's syndrome with occipital encephalocele and absence of corpus callosum.

Authors:  R Gershoni-Baruch; T Nachlieli; J N Guilburd
Journal:  Childs Nerv Syst       Date:  1991-08       Impact factor: 1.475

2.  Central nervous system and cervical spine abnormalities in Apert syndrome.

Authors:  Omar Breik; Antony Mahindu; Mark H Moore; Cindy J Molloy; Stephen Santoreneos; David J David
Journal:  Childs Nerv Syst       Date:  2016-02-10       Impact factor: 1.475

Review 3.  Apert syndrome: magnetic resonance imaging (MRI) of associated intracranial anomalies.

Authors:  Ai Peng Tan; Kshitij Mankad
Journal:  Childs Nerv Syst       Date:  2017-12-02       Impact factor: 1.475
  3 in total

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