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

Journal of Endocrinological Investigation

Volumn 40, Issue 2, 2017, Pages 123-134

  Bonomi, Marco ⁱ   Rochira, Vincenzo ⁱ   Pasquali, Daniela ⁱ   Balercia, Giancarlo ⁱ   Jannini, E A ^g   Ferlin, Alberto ⁱ   Calogero, Aldo ⁱ   Corona, Giovanni ⁱ   Fabbri, Andrea ⁱ   Francavilla, Felice ⁱ   Giagulli, Vito ⁱ   Lanfranco, Fabio ⁱ   Maggi, Mario ⁱ   Pivonello, Rosario ⁱ   Pizzocaro, Alessandro ⁱ   Radicioni, Antonio ⁱ   Accardo, Linda ⁱ   Cangiano, Biagio ⁱ   Condorelli, Rosita A ⁱ   Cordeschi, Giuliana ⁱ   D’Andrea, Settimio ⁱ   Mambro, Antonella Di ⁱ   Esposito, Daniela ⁱ   Foresta, Carlo ⁱ   Francavilla, Sandro ⁱ   Galdiero, Mariano ⁱ   Garolla, Andrea ⁱ   Giovannini, Lara ⁱ   Balercia, Antonio R M ⁱ   La Vignera, Sandro ⁱ   Motta, Giovanna ⁱ   Luciano, Luciano ⁱ   Pelliccione, Fiore ⁱ   Persani, Luca ⁱ   Santi, Daniele ⁱ   Selice, Riccardo ⁱ   Simoni, Manuela ⁱ   Tatone, Carla ⁱ   Tirabassi, Giacomo ⁱ   Tresoldi, Alberto Stefano ⁱ   Vicari, Enzo ⁱ   more..

^a UNIVERSITY OF MILAN   (Italy)

^b ISTITUTO AUXOLOGICO ITALIANO   (Italy)

^c UNIVERSITY OF MODENA AND REGGIO EMILIA   (Italy)

^d AUSL Modena   (Italy)

^e SECOND UNIVERSITY OF NAPLES   (Italy)

^f UNIVERSITÀ POLITECNICA DELLE MARCHE   (Italy)

^g UNIVERSITY OF ROME TOR VERGATA   (Italy)

^h UNIVERSITY OF PADOVA   (Italy)

ⁱ NONE

Author keywords

Azoospermia; Chromosome abnormalities; Hypergonadotropic hypogonadism; Klinefelter syndrome; KS; Male infertility; Testosterone

Indexed keywords

ANDROGEN RECEPTOR; TESTOSTERONE;

AGE; ANDROGEN DEFICIENCY; ANDROGEN THERAPY; CAG REPEAT; CLINICAL FEATURE; COPY NUMBER VARIATION; DISEASE SEVERITY; GENE DOSAGE; GENETIC BACKGROUND; GENETICS; HUMAN; HYPOGONADISM; KLINEFELTER SYNDROME; MALE; MALE INFERTILITY; MOSAICISM; NONHUMAN; PATHOGENESIS; PHENOTYPE; PSEUDOAUTOSOMAL REGION; REVIEW; SOMATIC CELL; SUPERNUMERARY CHROMOSOME; TESTOSTERONE BLOOD LEVEL; X CHROMOSOME; X CHROMOSOME INACTIVATION; PATHOLOGY;

HUMANS; HYPOGONADISM; KLINEFELTER SYNDROME; PHENOTYPE;

EID: 85010868140     PISSN: 03914097     EISSN: 17208386     Source Type: Journal    
DOI: 10.1007/s40618-016-0541-6     Document Type: Review

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