Literature DB >> 20843200

Klinefelter syndrome: clinical and molecular aspects.

Jacques C Giltay1, Merel C Maiburg.   

Abstract

Klinefelter syndrome is the most common chromosome abnormality in humans. The estimated prevalence is one in 500 to one in 1000 males but due to the widely variable and often aspecific features, only one in four cases are recognized. The most specific clinical features which can be observed at adult age are small testes, gynecomastia, female distribution of fat and body hair, slightly increased body length due to an increased leg length and azoospermia. Cognition is characterized by verbal deficits and psychosocial features include autistiform behavior. Structural brain abnormalities have been observed by MRI, such as decreased brain volumes and a decrease of asymmetry in areas corresponding to language performance. In the vast majority of cases a non-mosaic 47,XXY karyotype is observed. Parental imprinting of the extra X chromosome, variable inactivation of some X-chromosomal genes and CAG repeat length polymorphism of the androgen receptor may all be related to the variability of the phenotype. Surgical procedures of obtaining sperm in combination with repeated intracytoplasmic sperm injection/in vitro fertilization treatment may allow up to one in four men with Klinefelter syndrome to father children.

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Year:  2010        PMID: 20843200     DOI: 10.1586/erm.10.63

Source DB:  PubMed          Journal:  Expert Rev Mol Diagn        ISSN: 1473-7159            Impact factor:   5.225


  14 in total

1.  Aberrant gene expression profiles in pluripotent stem cells induced from fibroblasts of a Klinefelter syndrome patient.

Authors:  Yu Ma; Chunliang Li; Junjie Gu; Fan Tang; Chun Li; Peng Li; Ping Ping; Shi Yang; Zheng Li; Ying Jin
Journal:  J Biol Chem       Date:  2012-09-27       Impact factor: 5.157

2.  A man with Klinefelter's syndrome and new abdominal distension: a discussion of evaluation and management.

Authors:  Michael Postow; Manish A Shah; Maeve Lowery; Ali Shamseddine; Aghiad El-Kutoubi; Ashwaq Al Olayan; Mohamed Naghy; Celina Ang; Sally Tamraz; Abdul-Rahman Jazieh; Eileen M O'Reilly; David P Kelsen; Ghassan K Abou-Alfa
Journal:  J Gastrointest Cancer       Date:  2012-06

3.  Effect of sex chromosome number variation on attention-deficit/hyperactivity disorder symptoms, executive function, and processing speed.

Authors:  Tamar Green; Shira Flash; Geeta Shankar; Sharon Bade Shrestha; Booil Jo; Megan Klabunde; David S Hong; Allan L Reiss
Journal:  Dev Med Child Neurol       Date:  2021-08-24       Impact factor: 5.449

4.  Attitudes of Klinefelter men and their relatives towards TESE-ICSI.

Authors:  Merel C Maiburg; Alissia C Hoppenbrouwers; Henk F van Stel; Jacques C Giltay
Journal:  J Assist Reprod Genet       Date:  2011-06-30       Impact factor: 3.412

Review 5.  Mouse models of aneuploidy.

Authors:  Olivia Sheppard; Frances K Wiseman; Aarti Ruparelia; Victor L J Tybulewicz; Elizabeth M C Fisher
Journal:  ScientificWorldJournal       Date:  2012-01-03

6.  No influence of parental origin of intact X chromosome and/or Y chromosome sequences on three-year height response to growth hormone therapy in Turner syndrome.

Authors:  Hye Jin Lee; Hae Woon Jung; Gyung Min Lee; Hwa Young Kim; Jae Hyun Kim; Sun Hee Lee; Ji Hyun Kim; Young Ah Lee; Choong Ho Shin; Sei Won Yang
Journal:  Ann Pediatr Endocrinol Metab       Date:  2014-09-30

7.  Spontaneous pelvic rupture as a result of renal colic in a patient with klinefelter syndrome.

Authors:  Sergey Reva; Yuri Tolkach
Journal:  Case Rep Urol       Date:  2013-03-26

8.  Early developmental impact of sex chromosome trisomies on attention deficit-hyperactivity disorder symptomology in young children.

Authors:  Kimberly Kuiper; Hanna Swaab; Nicole Tartaglia; Sophie van Rijn
Journal:  Am J Med Genet A       Date:  2021-07-08       Impact factor: 2.578

9.  Can attention deficits predict a genotype? Isolate attention difficulties in a boy with klinefelter syndrome effectively treated with methylphenidate.

Authors:  Antonella Gagliano; Eva Germanò; Loredana Benedetto; Gabriele Masi
Journal:  Case Rep Pediatr       Date:  2014-08-19

10.  Neural systems for social cognition: gray matter volume abnormalities in boys at high genetic risk of autism symptoms, and a comparison with idiopathic autism spectrum disorder.

Authors:  Marcia N Goddard; Hanna Swaab; Serge A R B Rombouts; Sophie van Rijn
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2015-08-02       Impact factor: 5.270

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