Literature DB >> 1536180

Baller-Gerold syndrome: case report and clinical and radiological review.

B Dallapiccola1, L Zelante, R Mingarelli, M Pellegrino, V Bertozzi.   

Abstract

The major manifestations of the Baller-Gerold syndrome (BGS) are craniosynostosis and preaxial limb anomaly involving the radius and/or the thumb. We report on a new patient with coronal and sagittal suture involvement, mild unilateral radial and thumb hypoplasia, imperforate anus, rectovaginal fistula, prenatal onset growth deficiency, and mental retardation. This patient also had some minor oral-facial anomalies, severe nonfamilial myopia, bilateral conductive hearing loss, ureteric reflux, and skeletal anomalies other than those noted in the skull and upper limbs. This patient confirms the clinical variability among the patients and the wide pleiotropic effects of the BGS gene.

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Year:  1992        PMID: 1536180     DOI: 10.1002/ajmg.1320420323

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


  4 in total

1.  Ultrasound and MR imaging findings in prenatal diagnosis of craniosynostosis syndromes.

Authors:  Eva I Rubio; Anna Blask; Dorothy I Bulas
Journal:  Pediatr Radiol       Date:  2016-02-25

Review 2.  Baller-Gerold syndrome associated with congenital portal venous malformation.

Authors:  R Savarirayan; P Tomlinson; E Thompson
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

3.  Fetal exposure to sodium valproate associated with Baller-Gerold syndrome: case report and review of the literature.

Authors:  Ricardo Santos de Oliveira; Elizabeth Lajeunie; Eric Arnaud; Dominique Renier
Journal:  Childs Nerv Syst       Date:  2005-03-23       Impact factor: 1.475

Review 4.  Phenotypic variability in the Baller-Gerold syndrome: report of a mildly affected patient and review of the literature.

Authors:  F J Ramos Fuentes; L Nicholson; C I Scott
Journal:  Eur J Pediatr       Date:  1994-07       Impact factor: 3.183

  4 in total

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