A boy presenting with familial short stature - Diagnosis Gitelman syndrome

被引:0
作者
Schoof, E [1 ]
Marx, M [1 ]
Doerr, HG [1 ]
机构
[1] Univ Erlangen Nurnberg, Div Pediat Endocrinol, Hosp Children & Adolescents, D-91054 Erlangen, Germany
关键词
Gitelman syndrome; short stature;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patients with Gitelman syndrome are usually diagnosed by chance or present with muscular weakness, constipation, or tetanies due to hypokalemia and hypomagnesemia. We present a short statured boy with a clear history of familial short stature, normal growth and a final height prognosis within the target height range. However, routine laboratory studies led to the diagnosis of Gitelman syndrome, If a baseline laboratory analysis had not been performed, this diagnosis would have been missed.
引用
收藏
页码:891 / 894
页数:4
相关论文
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