Klinefelter syndrome and its variants: An update and review for the primary pediatrician

被引:66
|
作者
Visootsak, J
Aylstock, M
Graham, JM
机构
[1] Univ Calif Los Angeles, Ctr Med Genet Birth Defects,Steven Spielberg Pedi, Cedars Sinai Med Ctr,Ahmanson Pediat Ctr, Sch Med,Dept Pediat,SHAREs Child Disabil Ctr, Los Angeles, CA 90048 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Pediat, King Drew Med Ctr,Div Child Dev, Los Angeles, CA 90024 USA
[3] Klinefelter Syndrome & Associates, Roseville, CA USA
关键词
D O I
10.1177/000992280104001201
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Klinefelter syndrome is the most common chromosomal abnormality in humans. Recent prospective, unbiased studies have clarified many of the previous misconceptions associated with Klinefelter syndrome, thereby improving our recognition and management of this condition for affected individuals. The primary care physician has an important role in caring for these individuals and their families by providing anticipatory guidance regarding issues relating to endocrinology, behavior, development, and preventive medical care. Furthermore, the primary-care giver can serve as a valuable source of support and advocacy for the family of a boy with Klinefelter syndrome. We review the current state of knowledge regarding Klinefelter syndrome and its variants, with an emphasis on medical and early developmental interventions.
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页码:639 / 651
页数:13
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