Literature DB >> 7645600

Mixed sclerosing bone dysplasia, small stature, seizure disorder, and mental retardation: a syndrome?

S B Jurenka1, M I Van Allen.   

Abstract

We present a 40-year-old man with mental retardation, short stature, minor anomalies, and seizures, who was found to have osteopoikilosis with melorheostosis (mixed sclerosing bone dysplasia, MSBD). Cytogenetic findings of a low level trisomy 8 mosaicism were not confirmed by fluorescence in situ hybridization (FISH) of fibroblast cells. To our knowledge, the association of MSBD and mental retardation has not been previously reported.

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Year:  1995        PMID: 7645600     DOI: 10.1002/ajmg.1320570103

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


  5 in total

1.  A case of osteopoikilosis coexisting with amyloidosis of familial Mediterranean fever.

Authors:  Salih Kavukçu; Alper Soylu; Mehmet Türkmen; Dilek Güneş; Seymen Bora; Hüseyin Gülay
Journal:  Pediatr Nephrol       Date:  2003-10-30       Impact factor: 3.714

2.  Osteopoikilosis, short stature and mental retardation as key features of a new microdeletion syndrome on 12q14.

Authors:  Björn Menten; Karen Buysse; Farah Zahir; Jan Hellemans; Sara J Hamilton; Teresa Costa; Carrie Fagerstrom; George Anadiotis; Daniel Kingsbury; Barbara C McGillivray; Marco A Marra; Jan M Friedman; Frank Speleman; Geert Mortier
Journal:  J Med Genet       Date:  2007-01-12       Impact factor: 6.318

3.  The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growth.

Authors:  Sally Ann Lynch; Nicola Foulds; Ann-Charlotte Thuresson; Amanda L Collins; Göran Annerén; Bernt-Oves Hedberg; Carol A Delaney; James Iremonger; Caroline M Murray; John A Crolla; Colm Costigan; Wayne Lam; David R Fitzpatrick; Regina Regan; Sean Ennis; Freddie Sharkey
Journal:  Eur J Hum Genet       Date:  2011-01-26       Impact factor: 4.246

4.  Klippel-Feil syndrome with osteopoikilosis in a young lady and her four female relatives with osteopoikilosis.

Authors:  Serdar Toker; Volkan Kilincoglu; Koray Unay; Erden Erturer; Figen Taser; Erim Gulcan; Demet Ilhan
Journal:  Clin Rheumatol       Date:  2008-12-05       Impact factor: 2.980

5.  Refinement of the 12q14 microdeletion syndrome: primordial dwarfism and developmental delay with or without osteopoikilosis.

Authors:  Francesca Mari; Pia Hermanns; Maria L Giovannucci-Uzielli; Fiorella Galluzzi; Daryl Scott; Brendan Lee; Alessandra Renieri; Sheila Unger; Bernhard Zabel; Andrea Superti-Furga
Journal:  Eur J Hum Genet       Date:  2009-03-11       Impact factor: 4.246

  5 in total

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