Literature DB >> 7573131

Patient with craniosynostosis and marfanoid phenotype (Shprintzen-Goldberg syndrome) and cloverleaf skull.

H M Saal1, D I Bulas, J F Allen, L G Vezina, D Walton, K N Rosenbaum.   

Abstract

Marfanoid phenotype with craniosynostosis (Shprintzen-Goldberg syndrome) is a rare disorder previously described in only 5 patients. We report on the sixth known patient with this condition. The findings which distinguish our patient from others reported previously are that she was ascertained prenatally as having a cloverleaf skull; this is the first female patient described with this condition. Postnatally, she presented with arachnodactyly, camptodactyly, and clover-leaf skull. Imaging studies of the brain documented microcephaly with malformed brain, hydrocephaly, and hypoplasia of the corpus callosum. She also had choanal atresia and stenosis, a clinical finding previously reported only once, in this disorder.

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Year:  1995        PMID: 7573131     DOI: 10.1002/ajmg.1320570411

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


  2 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
  2 in total

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