Radiological and orthopedic abnormalities in Satoyoshi syndrome

被引:14
作者
Haymon, ML
Willis, RB
Ehlayel, MS
Lacassie, Y
机构
[1] LOUISIANA STATE UNIV, MED CTR, DEPT PEDIAT, DIV GENET, NEW ORLEANS, LA 70112 USA
[2] CHILDRENS HOSP, DEPT RADIOL, NEW ORLEANS, LA USA
[3] CHILDRENS HOSP, DEPT ORTHOPED, NEW ORLEANS, LA USA
[4] CHILDRENS HOSP, DEPT PEDIAT, NEW ORLEANS, LA USA
[5] LOUISIANA STATE UNIV, MED CTR, CTR MOL & HUMAN GENET, NEW ORLEANS, LA USA
关键词
MUSCLE SPASM; ALOPECIA; DIARRHEA;
D O I
10.1007/s002470050158
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Satoyoshi syndrome is a rare disorder of unknown etiology characterized by progressive, painful intermittent muscle spasms, severe skeletal abnormalities mimicking a skeletal dysplasia, malabsorption, alopecia, and amenorrhea. We further report on a 20 1/2-year-old Caucasian woman with characteristic manifestations of the syndrome. Since the establishment of the diagnosis 1 year ago, she has been treated with prednisone with good response, However, treatment of the multiple deformities and fractures has been difficult and challenging. The early recognition and treatment of this disorder is of utmost importance, as the skeletal deformities and fractures seem to be secondary to the muscular spasms, as suggested by Satoyoshi.
引用
收藏
页码:415 / 418
页数:4
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