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致死型低磷酸酯酶症中的特定骨赘与三维产前超声图像相关。

Specific osseous spurs in a lethal form of hypophosphatasia correlated with 3D prenatal ultrasonographic images.

作者信息

Sinico M, Levaillant J M, Vergnaud A, Blondeau J R, Encha-Razavi F, Mornet E, Le Merrer M, Gerard-Blanluet M

机构信息

Fetopathology, CHIC, Créteil, France.

出版信息

Prenat Diagn. 2007 Mar;27(3):222-7. doi: 10.1002/pd.1648.

Abstract

BACKGROUND

Hypophosphatasia is an osseous dysplasia with highly variable clinical expression, ranging from a recessive lethal prenatal type to late onset dominant short stature with premature shedding of teeth. Lethal forms of hypophosphatasia include short limb dwarfism with lack of ossification, especially on the vertebral bodies, very slender ribs and clavicles, and bowed, short lower extremities, with a bifid aspect of the diaphyses. Alkaline phosphatase is abnormally low in liver, bone, kidney and plasma.

METHODS

We present here the prenatal images of a lethal form of hypophosphatasia, diagnosed precociously because of specific osseous spurs in a context of recurrent short limb dwarfism.

RESULTS

Prenatal 3D ultrasonography has shown these spurs as early as 18 weeks. Molecular biology found compound heterozygous mutations in the gene TNSALP.

CONCLUSION

In a context of short limb dwarfism, the search for these specific osseous spurs orient strongly toward the diagnosis of lethal hypophosphatasia.

摘要

背景

低磷酸酯酶症是一种骨发育异常疾病,临床表现高度可变,从隐性致死性产前型到迟发性显性身材矮小伴牙齿过早脱落。低磷酸酯酶症的致死形式包括短肢侏儒症,伴有骨化缺失,尤其是椎体,肋骨和锁骨非常纤细,下肢弯曲且短,骨干有双叉状外观。肝脏、骨骼、肾脏和血浆中的碱性磷酸酶异常低。

方法

我们在此展示一种致死性低磷酸酯酶症的产前影像,由于在反复出现短肢侏儒症的情况下出现特定的骨赘而被早期诊断。

结果

产前三维超声早在18周时就显示出这些骨赘。分子生物学发现TNSALP基因存在复合杂合突变。

结论

在短肢侏儒症的情况下,寻找这些特定的骨赘强烈指向致死性低磷酸酯酶症的诊断。

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