Literature DB >> 15616510

Bilateral reactive lymphoid hyperplasia of the orbit in a child with Russell-Silver syndrome.

Yen N T Dang1, In C Shin, Robert A Gordon, Zeynel A Karcioglu.   

Abstract

Russell-Silver syndrome (RSS) primarily includes intrauterine growth retardation, postnatal growth failure, body asymmetry, and craniofacial disproportion. Four types of malignancies have been reported in patients with RSS: craniopharyngioma, testicular seminoma, hepatocellular carcinoma, and Wilms tumor.

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Year:  2004        PMID： 15616510     DOI： 10.1016/j.jaapos.2004.09.005

Source DB:  PubMed          Journal:  J AAPOS        ISSN： 1091-8531            Impact factor:   1.220


  2 in total

1.  Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype.

Authors:  Jet Bliek; Paulien Terhal; Marie-José van den Bogaard; Saskia Maas; Ben Hamel; Georgette Salieb-Beugelaar; Marleen Simon; Tom Letteboer; Jasper van der Smagt; Hester Kroes; Marcel Mannens
Journal:  Am J Hum Genet       Date:  2006-03-01       Impact factor: 11.025

2.  A case of Silver-Russell syndrome (SRS): multiple pituitary hormone deficiency, lack of H19 hypomethylation and favourable growth hormone (GH) treatment response.

Authors:  Zoran S Gucev; Velibor Tasic; Aleksandra Jancevska; Ilija Kirovski
Journal:  J Genet       Date:  2009-08       Impact factor: 1.166
  2 in total

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