Literature DB >> 16504797

Steroid sulfatase deficiency with bilateral periventricular nodular heterotopia.

Hiroshi Ozawa1, Maki Osawa, Toshiro Nagai, Nobuo Sakura.   

Abstract

This report presents a case of steroid sulfatase deficiency with bilateral periventricular nodular heterotopia. A 13-year-old male was diagnosed as having steroid sulfatase deficiency because steroid sulfatase activity was not detected in his leukocytes. In deoxyribonucleic acid studies, steroid sulfatase locus and adjacent loci were found to be deleted in his deoxyribonucleic acid. Cranial magnetic resonance imaging revealed periventricular nodular heterotopia, disclosing an irregular contour of the lateral walls of the lateral ventricles due to small nodular masses that were isointense as to the gray matter. In steroid sulfatase deficiency patients, bilateral periventricular nodular heterotopia must be considered.

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Year:  2006        PMID: 16504797     DOI: 10.1016/j.pediatrneurol.2005.08.015

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  2 in total

1.  Periventricular heterotopia in common microdeletion syndromes.

Authors:  M van Kogelenberg; S Ghedia; G McGillivray; D Bruno; R Leventer; K Macdermot; J Nelson; L Nagarajan; J A Veltman; A P de Brouwer; R J McKinlay Gardner; H van Bokhoven; E P Kirk; S P Robertson
Journal:  Mol Syndromol       Date:  2010-01-08

2.  Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report.

Authors:  Ingrid Anne Mandy Schierz; Mario Giuffrè; Marcello Cimador; Maria Michela D'Alessandro; Gregorio Serra; Federico Favata; Vincenzo Antona; Ettore Piro; Giovanni Corsello
Journal:  Ital J Pediatr       Date:  2022-02-03       Impact factor: 2.638

  2 in total

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