Literature DB >> 16342850

Klinefelter syndrome.

Daniel J Wattendorf1, Maximilian Muenke.   

Abstract

To complement the 2005 Annual Clinical Focus on medical genomics, AFP is publishing a series of short reviews on genetic syndromes. This series was designed to increase awareness of these diseases so that family physicians can recognize and diagnose children with these disorders and understand the kind of care they might require in the future. This review discusses Klinefelter syndrome.

Entities:  

Mesh：

Year:  2005        PMID： 16342850

Source DB:  PubMed          Journal:  Am Fam Physician        ISSN： 0002-838X            Impact factor:   3.292


  7 in total

1.  47,XXY/48,XXXY/49,XXXXY mosaic with hydrocephaly: a case report and review of the literature.

Authors:  Jesús E Dueñas-Arias; Maribel Aguilar-Medina; Eliakym Arámbula-Meraz; Juliana B Valenzuela-Camacho; Angelina Vega-Solano; Julio Granados; Rosalío Ramos-Payán
Journal:  J Med Case Rep       Date:  2007-09-19

Review 2.  Structural and functional neuroimaging in Klinefelter (47,XXY) syndrome: a review of the literature and preliminary results from a functional magnetic resonance imaging study of language.

Authors:  Kyle Steinman; Judith Ross; Song Lai; Allan Reiss; Fumiko Hoeft
Journal:  Dev Disabil Res Rev       Date:  2009

3.  Neuroanatomical phenotype of Klinefelter syndrome in childhood: a voxel-based morphometry study.

Authors:  Daniel M Bryant; Fumiko Hoeft; Song Lai; John Lackey; David Roeltgen; Judith Ross; Allan L Reiss
Journal:  J Neurosci       Date:  2011-05-04       Impact factor: 6.167

4.  A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.

Authors:  Ian Whitmarsh; Arlene M Davis; Debra Skinner; Donald B Bailey
Journal:  Soc Sci Med       Date:  2007-06-11       Impact factor: 4.634

5.  Autism spectrum disorder, Klinefelter syndrome, and chromosome 3p21.31 duplication: a case report.

Authors:  Scott W Stuart; Casey H King; G Shashidar Pai
Journal:  MedGenMed       Date:  2007-12-18

Review 6.  Klinefelter syndrome (KS): genetics, clinical phenotype and hypogonadism.

Authors:  M Bonomi; V Rochira; D Pasquali; G Balercia; E A Jannini; A Ferlin
Journal:  J Endocrinol Invest       Date:  2016-09-19       Impact factor: 4.256

7.  Regional differences in dosage compensation on the chicken Z chromosome.

Authors:  Esther Melamed; Arthur P Arnold
Journal:  Genome Biol       Date:  2007       Impact factor: 13.583
  7 in total

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