Abstract
Klinefelter syndrome (KS) is the most frequent sex chromosome disorder in males, but the phenotype varies greatly and is therefore highly under-diagnosed. We aimed at describing the phenotypic characteristics throughout life from clinical follow-up of our large cohort of patients with KS.
Originalsprog | Engelsk |
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Tidsskrift | Acta Paediatrica |
Vol/bind | 100 |
Udgave nummer | 6 |
Sider (fra-til) | 793-806 |
Antal sider | 14 |
ISSN | 0803-5253 |
DOI | |
Status | Udgivet - 1 jun. 2011 |