A Case of Malignant Pheochromocytoma with Holt-Oram Syndrome
Author:
Affiliation:
1. Department of Medicine, Institute of Clinical Endocrinology, Tokyo Women's Medical University
2. National Center of Child Health and Development
Publisher
Japan Endocrine Society
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
http://www.jstage.jst.go.jp/article/endocrj/55/1/55_K07E-011/_pdf
Reference32 articles.
1. 1. Frota Filho JD, Pereira W, Leiria TL, Vallenas M, Leaes PE, Blacher C, Lucio E, Lucchese FA (1999) Holt-Oram syndrome revisited. Two patients in the same family. Arq Bras Cardiol 73: 429-434.
2. 2. Brockhoff CJ, Kober H, Tsilimingas N, Dapper F, Munzel T, Meinertz T (1999) Holt-Oram syndrome. Circulation 99: 1395-1396.
3. 3. Bohm M (1998) Holt-Oram syndrome. Circulation 98: 2636-2637.
4. 4. Shono S, Higa K, Kumano K, Dan K (1998) Holt-Oram syndrome. Br J Anaesth 80: 856-857.
5. The Clinical and Genetic Spectrum of the Holt-Oram Syndrome (Heart-Hand Syndrome)
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2. Asymptomatic phaeochromocytoma in a patient with Holt-Oram syndrome: a case report;European Heart Journal - Case Reports;2019-11-09
3. Pheochromocytoma and paraganglioma in Fontan patients: Common more than expected;Congenital Heart Disease;2018-07
4. Pheochromocytoma complicated by cyanotic congenital heart disease: a case report;Clinical Pediatric Endocrinology;2016
5. Hypoxia Pathway Mutations in Pheochromocytomas and Paragangliomas;Cytogenetic and Genome Research;2016
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