Literature DB >> 3425612

Apparent G syndrome presenting as neck and upper limb dystonia and severe gastroesophageal reflux.

C A Williams1, J L Frias.   

Abstract

We have studied a 3-month-old boy with severe gastroesophageal reflux, feeding difficulties, neck and upper limb dystonia, abnormal ears, normal genitalia, and anatomically apparently normal larynx and trachea. Initially diagnosed as suffering from Sandifer "syndrome," he was treated with a gastrostomy and Nissen fundoplication. However, his characteristic facial appearance subsequently led to the diagnosis of G syndrome.

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Year:  1987        PMID: 3425612     DOI: 10.1002/ajmg.1320280206

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


  3 in total

1.  Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS.

Authors:  Donna M McDonald-McGinn; Somayyeh Fahiminiya; Timothée Revil; Beata A Nowakowska; Joshua Suhl; Alice Bailey; Elisabeth Mlynarski; David R Lynch; Albert C Yan; Larissa T Bilaniuk; Kathleen E Sullivan; Stephen T Warren; Beverly S Emanuel; Joris R Vermeesch; Elaine H Zackai; Loydie A Jerome-Majewska
Journal:  J Med Genet       Date:  2012-12-11       Impact factor: 6.318

2.  Treatment of Sandifer Syndrome with an Amino-Acid-Based Formula.

Authors:  Natasha Bamji; Stuart Berezin; Howard Bostwick; Marvin S Medow
Journal:  AJP Rep       Date:  2015-03-04

3.  Auditory findings and electrophysiologics in individuals with G/BBB syndrome.

Authors:  Tatiana Vialôgo Cassab; Sthella Zanchetta; Célia Maria Giacheti; Neivo Luiz Zorzetto; Antonio Richieri-Costa
Journal:  Braz J Otorhinolaryngol       Date:  2011 Nov-Dec
  3 in total

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