Klinefelter Syndrome in Childhood: Variability in Clinical and Molecular Findings | Zendy

Neşe Akcan | Zendy; Şükran Poyrazoğlu | Zendy; Firdevs Baş | Zendy; Rüveyde Bundak | Zendy; Feyza Darendelıler | Zendy

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Klinefelter Syndrome in Childhood: Variability in Clinical and Molecular Findings

Author(s) -

Neşe Akcan,

Şükran Poyrazoğlu,

Firdevs Baş,

Rüveyde Bundak,

Feyza Darendelıler

Publication year - 2017

Publication title -

journal of clinical research in pediatric endocrinology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.566

H-Index - 35

eISSN - 1308-5735

pISSN - 1308-5727

DOI - 10.4274/jcrpe.5121

Subject(s) - micropenis , medicine , klinefelter syndrome , short stature , pediatrics , disorders of sex development , hypospadias , bone age , neurocognitive , tall stature , genetic counseling , gynecology , psychiatry , surgery , genetics , cognition , biology

Klinefelter syndrome (KS) is the most common (1/500–1/1000) chromosomal disorder in males, but only 10% of cases are identified in childhood. This study aimed to review the data of children with KS to assess the age and presenting symptoms for diagnosis, clinical and laboratory findings, together with the presence of comorbidities.

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