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一个家族中的成人和婴儿型戈谢病:突变研究及临床进展

Adult and infantile Gaucher disease in one family: mutational studies and clinical update.

作者信息

Shahinfar M, Wenger D A

机构信息

Department of Medicine (Medical Genetics), Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania 19107.

出版信息

J Pediatr. 1994 Dec;125(6 Pt 1):919-21. doi: 10.1016/s0022-3476(05)82010-4.

Abstract

Molecular analysis and clinical updates are provided on a previously reported mother and adult son with Gaucher disease; two other children died with acute neuronopathic (type 2) Gaucher disease. The mother and son have the identical genotype (370/444) but very different clinical manifestations. These findings illustrate the need for additional studies before families with newly diagnosed Gaucher disease undergo counseling.

摘要

对先前报道的患有戈谢病的一位母亲和成年儿子进行了分子分析和临床更新;另外两个孩子死于急性神经元病变型(2型)戈谢病。母亲和儿子具有相同的基因型(370/444),但临床表现却大不相同。这些发现表明,在新诊断出戈谢病的家庭接受咨询之前,还需要进行更多研究。

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