Literature DB >> 3177455

Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome.

G Neri1, R Marini, M Cappa, P Borrelli, J M Opitz.   

Abstract

We report on another family with the so-called "gigantism-dysplasia syndrome", an X-linked condition characterized by pre- and postnatal overgrowth, characteristic face with apparent coarseness, dysplastic changes in several tissues, and mild intellectual impairment. This condition has been called the Golabi-Rosen syndrome; however, we agree that is the same entity as that described, in a milder form, by Simpson et al in 1975 and by Behmel et al in 1984. Therefore, we suggest that this entity be designated the Simpson-Golabi-Behmel syndrome. The manifestations in affected individuals suggest that this condition represents an X-linked encephalo-tropho-schisis syndrome.

Entities:  

Mesh:

Year:  1988        PMID: 3177455     DOI: 10.1002/ajmg.1320300130

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


  14 in total

1.  Glypican 3 overexpression in primary and metastatic Wilms tumors.

Authors:  Maria Tretiakova; Debra L Zynger; Chunyan Luan; Nicole K Andeen; Laura S Finn; Masha Kocherginsky; Bin T Teh; Ximing J Yang
Journal:  Virchows Arch       Date:  2014-11-04       Impact factor: 4.064

Review 2.  X linked mental retardation.

Authors:  I A Glass
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

3.  Microdissecting the genetic events in nephrogenic rests and Wilms' tumor development.

Authors:  A K Charles; K W Brown; P J Berry
Journal:  Am J Pathol       Date:  1998-09       Impact factor: 4.307

4.  Transient QT interval prolongation in an infant with Simpson-Golabi-Behmel syndrome.

Authors:  Emily Gertsch; Salman Kirmani; Michael J Ackerman; Dusica Babovic-Vuksanovic
Journal:  Am J Med Genet A       Date:  2010-09       Impact factor: 2.802

5.  Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes.

Authors:  J Eggenschwiler; T Ludwig; P Fisher; P A Leighton; S M Tilghman; A Efstratiadis
Journal:  Genes Dev       Date:  1997-12-01       Impact factor: 11.361

6.  Acid sphingomyelinase deficiency in Beckwith Wiedemann syndrome.

Authors:  L A Réthy ; R Kálmánchey ; V Klujber ; R Koós ; G Fekete
Journal:  Pathol Oncol Res       Date:  2000       Impact factor: 3.201

7.  Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

Authors:  S Lindsay; M Ireland; O O'Brien; J Clayton-Smith; J A Hurst; J Mann; T Cole; J Sampson; S Slaney; D Schlessinger; J Burn; G Pilia
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318

8.  Glypican-3-deficient mice exhibit developmental overgrowth and some of the abnormalities typical of Simpson-Golabi-Behmel syndrome.

Authors:  D F Cano-Gauci; H H Song; H Yang; C McKerlie; B Choo; W Shi; R Pullano; T D Piscione; S Grisaru; S Soon; L Sedlackova; A K Tanswell; T W Mak; H Yeger; G A Lockwood; N D Rosenblum; J Filmus
Journal:  J Cell Biol       Date:  1999-07-12       Impact factor: 10.539

Review 9.  Simpson-Golabi-Behmel syndrome types I and II.

Authors:  Jair Tenorio; Pedro Arias; Víctor Martínez-Glez; Fernando Santos; Sixto García-Miñaur; Julián Nevado; Pablo Lapunzina
Journal:  Orphanet J Rare Dis       Date:  2014-09-20       Impact factor: 4.123

10.  Gentle giant.

Authors:  Eswaradass Prasanna Venkatesan; Ramadoss Kalidoss; Balakrishnan Ramasamy; Gnanagurusamy Gnanashanmugham
Journal:  Ann Indian Acad Neurol       Date:  2015 Apr-Jun       Impact factor: 1.383

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