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Different Skeletal Phenotypes in a Mother and Two Daughters with ShortStature Homeobox-Containing Haploinsufficiency

机译:一位母亲和两个女儿矮的不同骨骼表型身材矮小的同源异型盒

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摘要

Haploinsufficiency of the short stature homeobox-containing (SHOX) gene causes Turner skeletal features such as short metacarpals, cubitus valgus, and Madelung deformity. We report the clinical findings of a Japanese family consisting of two daughters with SHOX haploinsufficiency (46, X, del(X) (p.22.3)) and their mother with 45,X [9]/ 46, X, del(X) (p22.3) [11] karyotype. Physical and auxological examinations revealed a mesomelic appearance, cubitus valgus, a short neck and short stature in the daughters, but on the other hand, only a short neck and short stature in the mother. Radiological studies indicated markedly curved radii in the daughters, but only mild curvature of the radii in the mother. Regular menstruation had taken place since the age of 12 yr in the elder daughter, but the mother had irregular menstruation and she had received fertility treatment for pregnancy. The different skeletal phenotypes of the mother and her daughters with SHOX haploinsufficiency might be due to the mild gonadal estrogen deficiency found in the mother, which was caused by mosaic Turner syndrome, and the phenotypic variability of SHOX haploinsufficiency.
机译:身材矮小的同源异型框(SHOX)基因的单倍剂量不足会导致特纳骨骼特征,如短掌骨,肘外翻和马德隆畸形。我们报告了一个日本家庭的临床发现,该家庭由两个SHOX单倍剂量不足的女儿(46,X,del(X)(p.22.3))和他们的母亲分别为45,X [9] / 46,X,del(X)组成(p22.3)[11]核型。体格检查和体格检查显示女儿呈梅索状外观,肘外翻,女儿的脖子短而矮小,但另一方面,母亲的脖子短而矮小。放射学研究表明,女儿的半径明显弯曲,但母亲的半径仅轻微弯曲。大女儿从12岁开始就定期进行月经,但是母亲的月经不规律,她接受了生育治疗。母亲和女儿患有SHOX单倍功能不全的骨骼型不同可能是由于母亲中发现的轻度性腺雌激素缺乏症,这是由镶嵌特纳综合征引起的,以及SHOX单倍功能不全的表型变异。

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