跳至主要内容
临床试验/JPRN-UMIN000010034
JPRN-UMIN000010034招募中未知

Genetic testing for Hereditary pheochromocytoma/ paraganglioma syndrome(HPPS) - Evaluation of genetic testing for HPPS

niversity of Tsukuba,Faculty of Medicine0 个研究点目标入组 900 人开始时间: 2013年2月15日最近更新:
适应症

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

研究者

发起方
niversity of Tsukuba,Faculty of Medicine

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