Literature DB >> 12846610

Shprintzen-Goldberg syndrome: case report.

N Topouzelis1, E Markovitsi, K Antoniades.   

Abstract

OBJECTIVE: The Shprintzen-Goldberg syndrome is an extremely rare syndrome with a characteristic face. This is one of a group of disorders characterized by craniosynostosis and marfanoid features. The aim of this study was to present a new sporadic case of the syndrome and describe in detail the findings at the maxillofacial region.

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Year:  2003        PMID： 12846610     DOI： 10.1597/1545-1569_2003_040_0433_sscr_2.0.co_2

Source DB:  PubMed          Journal:  Cleft Palate Craniofac J        ISSN： 1055-6656


  3 in total

1.  Shprintzen-Goldberg syndrome presenting as umbilical hernia in an Indian child.

Authors:  Bhushan Shah; Suman Sahu; Piyush Kalakoti; Sankalp Yadav; M M Aarif Syed; Venugopal Brijmohan Bhattad; Meena Shaikh
Journal:  Australas Med J       Date:  2014-02-28

Review 2.  Shprintzen-Goldberg syndrome: a rare disorder.

Authors:  Sankalp Yadav; Gautam Rawal
Journal:  Pan Afr Med J       Date:  2016-04-25

3.  Craniosynostosis, Scheuermann's disease, and intellectual disability resembling Shprintzen-Goldberg syndrome: a report on a family over 4 generations: Case report.

Authors:  Ali Al Kaissi; Zahra Marrakchi; Nabil M Nassib; Jochen Hofstaetter; Franz Grill; Rudolf Ganger; Susanne Gerit Kircher
Journal:  Medicine (Baltimore)       Date:  2017-03       Impact factor: 1.889
  3 in total

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