Literature DB >> 3529433

Klinefelter's syndrome: historical background and development.

H F Klinefelter.   

Abstract

When described more than 40 years ago, Klinefelter's syndrome (small testes, sterility, increased excretion of follicle-stimulating hormone, and usually gynecomastia) was thought to be an endocrine disorder. A second testicular hormone was postulated but has never been isolated. During the ensuing years, the syndrome has been found to be a chromosomal disorder, in which there is an extra X chromosome in 80% of the patients. The disorder occurs once in 500 to 1,000 male births and is best diagnosed by a buccal smear. When there is androgen deficiency, it is treated with testosterone. Gynecomastia is treated surgically because of the potential danger of malignancy or for cosmetic reasons.

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Year:  1986        PMID: 3529433

Source DB:  PubMed          Journal:  South Med J        ISSN: 0038-4348            Impact factor:   0.954


  6 in total

1.  Fluid intelligence, traits of personality and personality disorders in a cohort of adult KS patients with the classic 47, XXY karyotype.

Authors:  D Liberato; S Granato; D Grimaldi; F M Rossi; N Tahani; D Gianfrilli; A Anzuini; A Lenzi; G Cavaggioni; A F Radicioni
Journal:  J Endocrinol Invest       Date:  2017-04-11       Impact factor: 4.256

2.  An early description of Klinefelter syndrome at the beginning of the 20th century by Spyridon Livadas, an officer of the Medical Corps of the Hellenic Navy.

Authors:  A Diamantis; E Magiorkinis; L E Vladimiros; G Androutsos
Journal:  J Endocrinol Invest       Date:  2008-10       Impact factor: 4.256

3.  RABGAP1L gene rearrangement resulting from a der(Y)t(Y;1)(q12;q25) in acute myeloid leukemia arising in a child with Klinefelter syndrome.

Authors:  Maria Cristina Roberti; Roberta La Starza; Cecilia Surace; Pietro Sirleto; Rita Maria Pinto; Valentina Pierini; Barbara Crescenzi; Cristina Mecucci; Adriano Angioni
Journal:  Virchows Arch       Date:  2009-01-28       Impact factor: 4.064

4.  Klinefelter's Syndrome with Maternal Uniparental Disomy X, Interstitial Xp22.31 Deletion, X-linked Ichthyosis, and Severe Central Nervous System Regression.

Authors:  Jennifer Brault; Laurence Walsh; Gail H Vance; David D Weaver
Journal:  J Pediatr Genet       Date:  2020-08-20

Review 5.  Advances in the Interdisciplinary Care of Children with Klinefelter Syndrome.

Authors:  Shanlee Davis; Susan Howell; Rebecca Wilson; Tanea Tanda; Judy Ross; Philip Zeitler; Nicole Tartaglia
Journal:  Adv Pediatr       Date:  2016-08

6.  Shifting syndromes: Sex chromosome variations and intersex classifications.

Authors:  David Andrew Griffiths
Journal:  Soc Stud Sci       Date:  2018-02       Impact factor: 3.885

  6 in total

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