Letter to the Editor: Familial and early recurrent pheochromocytoma in a child with a novel in-frame duplication variant of .
作者信息
Sato Takeshi, Hanakawa Junko, Iwano Reiko, Muroya Koji
机构信息
Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Yokohama, Japan.
Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
出版信息
Clin Pediatr Endocrinol. 2025 Apr;34(2):149-150. doi: 10.1297/cpe.2025-0016. Epub 2025 Feb 23.
Abstract
摘要
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Letter to the Editor: Familial and early recurrent pheochromocytoma in a child with a novel in-frame duplication variant of .致编辑的信：一名患有新型框内重复变异的儿童的家族性和早期复发性嗜铬细胞瘤
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本文引用的文献
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Endocr J. 2025 Apr 1;72(4):399-412. doi: 10.1507/endocrj.EJ24-0584. Epub 2025 Feb 1.
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Familial and early recurrent pheochromocytoma in a child with a novel in-frame duplication variant of .一名患有新型框内重复变异的儿童的家族性和早期复发性嗜铬细胞瘤 。
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3
von Hippel-Lindau disease type 2A in a family with a duplicated 21-base-pair in-frame insertion mutation in the VHL gene.一个患有VHL基因21个碱基对框内重复插入突变的家族中的2A型希佩尔-林道病。
Graefes Arch Clin Exp Ophthalmol. 2003 Mar;241(3):241-4. doi: 10.1007/s00417-003-0631-y. Epub 2003 Feb 20.
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