Genetic testing for Hereditary pheochromocytoma/ paraganglioma syndrome(HPPS) - Evaluation of genetic testing for HPPS
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 900
研究概览
简要总结
Takeichi N,et al .Identical Germline Mutations in the TMEM127 Gene in 2 Unrelated Japanese Patients with Bilateral Pheochromocytoma. Clinical Endocrinology,77,7.7-714,2012 Kodama H, Iihara M, Nissato S, Isobe K, Kawakami Y, Okamoto T, Takekoshi K: A large deletion in the succinate dehydrogenase B gene (SDHB) in a Japanese patient with abdominal paraganglioma and concomitant metastasis. Endocrine Journal, 57, 351-356, 2010 Saito T, Saito Y, Matsumura K, Tsubota Y, Maniwa T, Kaneda H, Minami K, Sakaida N, Uemura Y, Kawa G, Yamamoto N, Fujii Y, Isobe K, Kawakami Y, Matsuda T, Takekoshi K: Novel mutation (L157X) in the succinate dehydrogenase B gene (SDHB) in a Japanese family with abdominal paraganglioma following lung metastasis. Endocrine Journal, 56, 451-458, 2009
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 16years-old 至 80years-old(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •under 16 years old
