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Update on Physical, Psychological, and Quality of Life Management in Klinefelter Syndrome.
J Clin Endocrinol MetabMehmet B +4 more
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Lancet, The, 2004
Klinefelter's syndrome is the most common genetic cause of human male infertility, but many cases remain undiagnosed because of substantial variation in clinical presentation and insufficient professional awareness of the syndrome itself. Early recognition and hormonal treatment of the disorder can substantially improve quality of life and prevent ...
Eberhard Nieschlag +2 more
exaly +5 more sources
Klinefelter's syndrome is the most common genetic cause of human male infertility, but many cases remain undiagnosed because of substantial variation in clinical presentation and insufficient professional awareness of the syndrome itself. Early recognition and hormonal treatment of the disorder can substantially improve quality of life and prevent ...
Eberhard Nieschlag +2 more
exaly +5 more sources
Lancet, The, 2000
Klinefelter’s syndrome (KS) is the most common sex chromosome disorder in men, affecting roughly 1 in 400–600 men throughout all ethnic groups (1,2) It is also the most common cause of primary testicular failure, resulting in impairments in both spermatogenesis and testosterone production.
Paulsen, C. Alvin +3 more
exaly +3 more sources
Klinefelter’s syndrome (KS) is the most common sex chromosome disorder in men, affecting roughly 1 in 400–600 men throughout all ethnic groups (1,2) It is also the most common cause of primary testicular failure, resulting in impairments in both spermatogenesis and testosterone production.
Paulsen, C. Alvin +3 more
exaly +3 more sources
BMJ, 2012
A 29 year old man presented to primary care with anxiety and depression that had worsened since childhood. Further questioning revealed a history of poor school performance, poor body image, and poor self esteem. On physical examination, the patient’s height was 189 cm and he had narrow shoulders, wide hips, sparse facial hair (which he shaved once ...
Christopher H, Blevins +1 more
openaire +2 more sources
A 29 year old man presented to primary care with anxiety and depression that had worsened since childhood. Further questioning revealed a history of poor school performance, poor body image, and poor self esteem. On physical examination, the patient’s height was 189 cm and he had narrow shoulders, wide hips, sparse facial hair (which he shaved once ...
Christopher H, Blevins +1 more
openaire +2 more sources
2021
• KS ist die häufigste chromosomale Störung bei Männern. • Die klinischen Symptome sind bei Patienten mit KS sehr heterogen, wobei eine stark beeinträchtigte Spermatogenese und Unterfunktion der Leydig-Zellen gemeinsame Merkmale sind, die zu Azoospermie und hypergonadotropem Hypogonadismus führen.
Lanfranco F., Marinelli L., Nieschlag E.
openaire +3 more sources
• KS ist die häufigste chromosomale Störung bei Männern. • Die klinischen Symptome sind bei Patienten mit KS sehr heterogen, wobei eine stark beeinträchtigte Spermatogenese und Unterfunktion der Leydig-Zellen gemeinsame Merkmale sind, die zu Azoospermie und hypergonadotropem Hypogonadismus führen.
Lanfranco F., Marinelli L., Nieschlag E.
openaire +3 more sources
Best Practice & Research Clinical Endocrinology & Metabolism, 2011
Klinefelter syndrome (KS) is the most common genetic form of male hypogonadism, but overt phenotype becomes evident only after puberty. During childhood, and even during early puberty, pituitary-gonadal function in 47,XXY subjects is relatively normal, but from midpuberty onwards, FSH and LH levels increase to hypergonadotropic levels, inhibin B ...
Anne M, Wikström, Leo, Dunkel
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Klinefelter syndrome (KS) is the most common genetic form of male hypogonadism, but overt phenotype becomes evident only after puberty. During childhood, and even during early puberty, pituitary-gonadal function in 47,XXY subjects is relatively normal, but from midpuberty onwards, FSH and LH levels increase to hypergonadotropic levels, inhibin B ...
Anne M, Wikström, Leo, Dunkel
openaire +2 more sources
Klinefelter Syndrome and Turner Syndrome
Pediatrics In Review, 20211. Carole Samango-Sprouse, EdD*,†,‡ 2. Sophia Q. Song, BA‡ 3. Angela E. Lin, MD§ 4. Cynthia M. Powell, MD¶ 5. Andrea L. Gropman, MD*,** 1. *George Washington University, Washington, DC 2. †Florida International University, Miami, FL 3. ‡Department of Research, The Focus Foundation, Davidsonville, MD 4.
Carole, Samango-Sprouse +4 more
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Spermatogenesis in Klinefelter's Syndrome
The Journal of Clinical Endocrinology & Metabolism, 1965Two patients with clinical evidence of Klinefelter's syndrome, positive sex chromatin and a karyotype of 47/XXY are presented. Testicular biopsy revealed a histological picture characteristic of Klinefelter's syndrome, but, in addition to this, small areas of spermatogenesis were encountered in a few tubules.
E, Steinberger, K D, Smith, W H, Perloff
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