Literature DB >> 8533797

Monozygotic twins discordant for the Russell-Silver syndrome.

W Bailey1, B Popovich, K L Jones.   

Abstract

Russell-Silver syndrome (RSS) is a pattern of malformation characterized by intrauterine and postnatal growth retardation, limb asymmetry, triangular face, and hypospadias. We report on a patient, from a triplet pregnancy, who was one of identical male twins discordant for RSS. R.B. was a 710-g male born at 33 weeks of gestation, with hypospadias, chordee, and undescended testes. He had a normal 46,XY karyotype and no renal abnormalities. Female triplet A weighed 1,843 g, and male triplet B weighed 1,920 g. Both had normal physical findings and neonatal period. R.B. was first seen by us at age 6 7/12 years with short stature, triangular and asymmetric face, lower limb length discrepancy, and surgically repaired genital anomalies. Growth hormone testing results were normal. At age 8 7/12 years the brothers appeared physically identical except for size, with a height differential of 114.25 vs. 121.5 cm. Testing to establish biological zygosity was performed using VNTR (variable number tandem repeat) DNA probes YNH24 (D2S44), CMM101 (D14S13), EFD52 (D17S26), TBQ7 (D10S28), and 3'HVR (D16S85), PCR loci MCT118 (D1S80), and HLA-DQ alpha. These data indicate a > 99.99% probability of triplets B and C being monozygotic twins. While most occurrences of RSS are sporadic, familial cases suggesting autosomal dominance have been reported. Three other cases of probable monozygotic twins with RSS have been described. The significance of this confirmation of discordance in determining the cause of RSS is discussed.

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Year:  1995        PMID: 8533797     DOI: 10.1002/ajmg.1320580202

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


  7 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.  Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci.

Authors:  Claire Louise Susan Turner; Deborah M Mackay; Jonathan L A Callaway; Louise E Docherty; Rebecca L Poole; Hilary Bullman; Margaret Lever; Bruce M Castle; Emma C Kivuva; Peter D Turnpenny; Sarju G Mehta; Sahar Mansour; Emma L Wakeling; Verghese Mathew; Jackie Madden; Justin H Davies; I Karen Temple
Journal:  Eur J Hum Genet       Date:  2010-01-27       Impact factor: 4.246

3.  Russell-Silver syndrome: twin presentation.

Authors:  Carlos G Teran; Patricia Villarroel; Carlos N Teran-Escalera
Journal:  BMJ Case Rep       Date:  2009-03-17

Review 4.  New developments in Silver-Russell syndrome and implications for clinical practice.

Authors:  Miho Ishida
Journal:  Epigenomics       Date:  2016-04-12       Impact factor: 4.778

Review 5.  Silver-Russell syndrome: genetic basis and molecular genetic testing.

Authors:  Thomas Eggermann; Matthias Begemann; Gerhard Binder; Sabrina Spengler
Journal:  Orphanet J Rare Dis       Date:  2010-06-23       Impact factor: 4.123

6.  Monozygotic female twins discordant for Silver-Russell syndrome and hypomethylation of the H19-DMR.

Authors:  Kazuki Yamazawa; Masayo Kagami; Maki Fukami; Keiko Matsubara; Tsutomu Ogata
Journal:  J Hum Genet       Date:  2008-08-16       Impact factor: 3.172

Review 7.  Cerebellar and Striatal Implications in Autism Spectrum Disorders: From Clinical Observations to Animal Models.

Authors:  Mathieu Thabault; Valentine Turpin; Alexandre Maisterrena; Mohamed Jaber; Matthieu Egloff; Laurie Galvan
Journal:  Int J Mol Sci       Date:  2022-02-18       Impact factor: 5.923

  7 in total

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