PTPN11 Gene Mutation Associated With Abnormal Gonadal Determination

被引:3
作者
Ghai, Shailly Jain [1 ,2 ]
Keating, Sarah [3 ]
Chitayat, David [1 ,2 ]
机构
[1] Univ Toronto, Prenatal Diag & Med Genet Program, Mt Sinai Hosp, Dept Obstet & Gynecol, Toronto, ON M5G 1Z5, Canada
[2] Univ Toronto, Div Clin & Metab Genet, Hosp Sick Children, Dept Pediat, Toronto, ON M5G 1Z5, Canada
[3] Univ Toronto, Mt Sinai Hosp, Dept Pathol & Lab Med, Toronto, ON M5G 1Z5, Canada
关键词
ambiguous genitalia; hydrops fetalis; noonan syndrome; PTPN11; NOONAN-SYNDROME; LEOPARD-SYNDROME; SHP-2; PHOSPHATASE;
D O I
10.1002/ajmg.a.33873
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Germline mutations in the PTPN11 gene have been associated with Noonan syndrome (NS) and LEOPARD syndrome. Both germline and somatic mutations in this gene have been reported in association with malignancies. However, the T507K mutation in the PTPN11 gene, has only been reported in malignancies and in a fetus with hydrops fetalis but not in a live patient with NS. We report the autopsy findings in a fetus with the T507K mutation who presented prenatally with hydrops fetalis, cystic hygroma and 46, XX karyotype. On autopsy, the patient was found to have testes, male external genitalia, but absent Wolffian ducts. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:1136 / 1139
页数:4
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