Familial case of pheochromocytoma due to Von Hippel Lindau (VHL) gene mutation

被引：0
|
作者：
Bogdanova, Polina S. [1 ]
Kuznetsova, Elvira S. [1 ]
Beltsevich, Dmitry G.
Troshina, Ekaterina A. [2 ]
Melikyan, Maria A. [1 ]
Peterkova, Valentina A. [1 ]
机构：
[1] Endocrinol Res Ctr, Inst Pediat Endocrinol, Moscow, Russia
[2] Endocrinol Res Ctr, Inst Clin Endocrinol, Moscow, Russia
来源：
HORMONE RESEARCH | 2009年 / 72卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：67 / 68
页数：2
相关论文
共 50 条
  • [1] Familial pheochromocytoma due to mutant von Hippel Lindau disease gene
    Mulvihill, JJ
    Ferrell, RE
    Carty, SE
    Tisherman, SE
    Zbar, B
    ARCHIVES OF INTERNAL MEDICINE, 1997, 157 (12) : 1390 - 1391
  • [2] Mutation screening of VHL gene in a family with malignant bilateral pheochromocytoma: from isolated familial pheochromocytoma to von Hippel-Lindau disease
    Hasani-Ranjbar, Shirin
    Amoli, Mahsa M.
    Ebrahim-Habibi, Azadeh
    Haghpanah, Vahid
    Hejazi, Maryam
    Soltani, Akbar
    Larijani, Bagher
    FAMILIAL CANCER, 2009, 8 (04) : 465 - 471
  • [3] Mutation screening of VHL gene in a family with malignant bilateral pheochromocytoma: from isolated familial pheochromocytoma to von Hippel-Lindau disease
    Shirin Hasani-Ranjbar
    Mahsa M. Amoli
    Azadeh Ebrahim-Habibi
    Vahid Haghpanah
    Maryam Hejazi
    Akbar Soltani
    Bagher Larijani
    Familial Cancer, 2009, 8 : 465 - 471
  • [4] Familial pheochromocytoma associated with a novel mutation in the von Hippel-Lindau gene
    Gross, DJ
    Avishai, N
    Meiner, V
    Filon, D
    Zbar, B
    Abeliovich, D
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (01): : 147 - 149
  • [5] Familial isolated pheochromocytoma presenting a new mutation in the von Hippel-Lindau gene
    Sansó, G
    Rudaz, MCG
    Levin, G
    Barontini, M
    AMERICAN JOURNAL OF HYPERTENSION, 2004, 17 (12) : 1107 - 1111
  • [6] Hereditary pheochromocytoma with the von Hippel-Lindau gene mutation in a child: A case report
    Zheng, Shengqi
    Yin, Guicao
    Zhou, Ming
    Li, Yifan
    ASIAN JOURNAL OF SURGERY, 2023, 46 (05) : 2256 - 2258
  • [7] Cerebral venous thrombosis due to pheochromocytoma in a patient with Von Hippel Lindau mutation
    Nambiar, Vivek K.
    Sajitha, S.
    Viswanath, Naveen
    Praveen, V. P.
    Bindhu, M. R.
    NEUROLOGY INDIA, 2017, 65 (03) : 643 - +
  • [8] Identification of a VHL gene mutation in a Chinese family with Von Hippel-Lindau syndrome
    He, Zhengwen
    Xia, Lu
    Deng, Zhiyong
    Lian, Aojie
    Hu, Zhengmao
    Li, Bin
    MOLECULAR MEDICINE REPORTS, 2018, 18 (01) : 435 - 440
  • [9] Germline mutation profile of the VHL gene in von Hippel Lindau disease and in sporadic hemangioblastoma
    Olschwang, S
    Richard, S
    Boisson, C
    Giraud, S
    Laurent-Puig, P
    Resche, F
    Thomas, G
    HUMAN MUTATION, 1998, 12 (06) : 424 - 430
  • [10] Biochemically normal adrenal pheochromocytoma following extensive central necrosis in a child with von Hippel-Lindau (VHL) gene mutation
    Ng, Benjamin Wei-Liang
    Wong, Jeanne Sze-Lyn
    Toh, Teck-Hock
    BMJ CASE REPORTS, 2021, 14 (12)
12345