Literature DB >> 2529272

Septo-optic dysplasia (SOD) or DeMorsier syndrome.

U Roessmann1.   

Abstract

The historical evolution of the DeMorsier syndrome is reviewed. As the emphasis shifted from the eye findings to endocrinological defects and as the syndrome was further expanded through more frequent and easier radiological examination, the concept appears to have expanded, raising questions as to the nature of the disease and its clinical expression. To determine pathogenesis and better define the extent of the disease, further observations are needed, including postmortem studies on patients with septo-optic dysplasia and related disorders.

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Mesh:

Year:  1989        PMID: 2529272

Source DB:  PubMed          Journal:  J Clin Neuroophthalmol        ISSN: 0272-846X


  4 in total

Review 1.  HESX1 and Septo-Optic Dysplasia.

Authors:  Mehul Tulsidas Dattani; Iain Caf Robinson
Journal:  Rev Endocr Metab Disord       Date:  2002-12       Impact factor: 6.514

Review 2.  The role of homeodomain transcription factors in heritable pituitary disease.

Authors:  Kelly L Prince; Emily C Walvoord; Simon J Rhodes
Journal:  Nat Rev Endocrinol       Date:  2011-07-26       Impact factor: 43.330

3.  Bilateral anophthalmia with septo-optic dysplasia.

Authors:  Manisha Jana; Sanjay Sharma
Journal:  Oman J Ophthalmol       Date:  2010-05

Review 4.  Genetics of septo-optic dysplasia.

Authors:  Daniel Kelberman; Mehul Tulsidas Dattani
Journal:  Pituitary       Date:  2007       Impact factor: 4.107

  4 in total

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