Neurofibromatosis Type 1 with Overlap Turner Syndrome and Klinefelter Syndrome

被引:6
作者
Hatipoglu, Nihal [1 ]
Kurtoglu, Selim [2 ]
Kendirci, Mustafa [2 ]
Keskin, Mehmet [3 ]
Per, Hueseyin [4 ]
机构
[1] Sisli Etfal Res & Educ Hospital, Dept Pediat Endocrinol, Istanbul, Turkey
[2] Erciyes Univ, Dept Pediat Endocrinol, Fac Med, Kayseri, Turkey
[3] Gaziantep Univ, Dept Pediat Endocrinol, Fac Med, Gaziantep, Turkey
[4] Erciyes Univ, Dept Pediat Neurol, Fac Med, Kayseri, Turkey
关键词
turner syndrome; klinefelter syndrome; Neurofibromatosis type 1; NOONAN-SYNDROME; DIAGNOSIS; FAMILY;
D O I
10.1093/tropej/fmp053
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Turner's syndrome is a sex chromosome disorder. Klinefelter's syndrome is one of the most severe genetic diseases. Neurofibromatosis is an autosomal dominant disorder characterized by cafe-au-lait spots and fibromatous tumors of the skin. In this article, we report the overlap of neurofibromatosis-1 with Turner and Klinefelter syndromes. Thus, these disorders might overlap within the same patient. Due to these cases, we suggest that each patient with Turner-like symptoms or Klinefelter's-like syndrome, be carefully examined for cafe au lait macules before the initiation of hormone replacement treatment.
引用
收藏
页码:69 / 72
页数:4
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