Literature DB >> 9007334

Cerebral defects confirm midline developmental field disturbances in supernumerary der(22), t(11;22) syndrome.

R Pallotta1, P Fusilli, T Ehresmann, R Cinti, A Verrotti, G Morgese.   

Abstract

We describe a girl with midline defects and distal limb anomalies, who had a supernumerary der(22) syndrome. The presence of some anomalies identifying the midline defects, led us to review all patients reported up to now, with interesting results. We point out the particular finding of midline defects in CNS only, in patients studied by autopsy or neuroradiologic imaging.

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Year:  1996        PMID: 9007334     DOI: 10.1111/j.1399-0004.1996.tb02398.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  2 in total

Review 1.  Phenotypic characterization of derivative 22 syndrome: case series and review.

Authors:  Deepti Saxena; Priyanka Srivastava; Moni Tuteja; Kausik Mandal; Shubha R Phadke
Journal:  J Genet       Date:  2018-03       Impact factor: 1.166

2.  Phenotypic delineation of Emanuel syndrome (supernumerary derivative 22 syndrome): Clinical features of 63 individuals.

Authors:  Melissa T Carter; Stephanie A St Pierre; Elaine H Zackai; Beverly S Emanuel; Kym M Boycott
Journal:  Am J Med Genet A       Date:  2009-08       Impact factor: 2.802

  2 in total

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