Literature DB >> 11771918

Klinefelter syndrome and its variants: an update and review for the primary pediatrician.

J Visootsak1, M Aylstock, J M Graham.   

Abstract

Klinefelter syndrome is the most common chromosomal abnormality in humans. Recent prospective, unbiased studies have clarified many of the previous misconceptions associated with Klinefelter syndrome, thereby improving our recognition and management of this condition for affected individuals. The primary-care physician has an important role in caring for these individuals and their families by providing anticipatory guidance regarding issues relating to endocrinology, behavior, development, and preventive medical care. Furthermore, the primary-care giver can serve as a valuable source of support and advocacy for the family of a boy with Klinefelter syndrome. We review the current state of knowledge regarding Klinefelter syndrome and its variants, with an emphasis on medical and early developmental interventions.

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Year:  2001        PMID: 11771918     DOI: 10.1177/000992280104001201

Source DB:  PubMed          Journal:  Clin Pediatr (Phila)        ISSN: 0009-9228            Impact factor:   1.168


  18 in total

Review 1.  Consensus statement on diagnosis and clinical management of Klinefelter syndrome.

Authors:  A F Radicioni; A Ferlin; G Balercia; D Pasquali; L Vignozzi; M Maggi; C Foresta; A Lenzi
Journal:  J Endocrinol Invest       Date:  2010-12       Impact factor: 4.256

2.  X-chromosome dosage affects male sexual behavior.

Authors:  Paul J Bonthuis; Kimberly H Cox; Emilie F Rissman
Journal:  Horm Behav       Date:  2012-02-10       Impact factor: 3.587

3.  Two patients with intraspinal germinoma associated with Klinefelter syndrome: case report and review of the literature.

Authors:  Y Nakata; A Yagishita; N Arai
Journal:  AJNR Am J Neuroradiol       Date:  2006 Jun-Jul       Impact factor: 3.825

4.  Congenital defect of the partial atrioventricular canal with Klinefelter syndrome.

Authors:  Yejing Zhang
Journal:  BMJ Case Rep       Date:  2009-12-22

5.  [35-year old patient with severe thromboembolism].

Authors:  J-G Kluge; I Körner; G Kluge; U Froster; D Pfeiffer
Journal:  Internist (Berl)       Date:  2010-12       Impact factor: 0.743

6.  Social function in multiple X and Y chromosome disorders: XXY, XYY, XXYY, XXXY.

Authors:  Jeannie Visootsak; John M Graham
Journal:  Dev Disabil Res Rev       Date:  2009

7.  Diagnosis of variant klinefelter syndrome in a 21-year-old male who presented with sparse facial hair.

Authors:  Seda Purnak; Simin Ada; A Tülin Güleç; Tugce Bulakbasi Balci; Feride Iffet Sahin
Journal:  Ann Dermatol       Date:  2012-07-25       Impact factor: 1.444

8.  Two boys with 47, XXY and autism.

Authors:  S L Merhar; P Manning-Courtney
Journal:  J Autism Dev Disord       Date:  2007-05

9.  Non-organ-specific autoimmunity in adult 47,XXY Klinefelter patients and higher-grade X-chromosome aneuploidies.

Authors:  Francesca Panimolle; Claudio Tiberti; Matteo Spaziani; Gloria Riitano; Giuseppe Lucania; Antonella Anzuini; Andrea Lenzi; Daniele Gianfrilli; Maurizio Sorice; Antonio F Radicioni
Journal:  Clin Exp Immunol       Date:  2021-06-10       Impact factor: 5.732

Review 10.  Klinefelter syndrome and other sex chromosomal aneuploidies.

Authors:  Jeannie Visootsak; John M Graham
Journal:  Orphanet J Rare Dis       Date:  2006-10-24       Impact factor: 4.123

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