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MINERVA PEDIATRICA

A Journal on Pediatrics, Neonatology, Adolescent Medicine,
Child and Adolescent Psychiatry


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Minerva Pediatrica 2017 August;69(4):370-2

DOI: 10.23736/S0026-4946.16.04434-X

Copyright © 2016 EDIZIONI MINERVA MEDICA

language: English

Purpura Fulminans as the presenting manifestation in a patient with homozygous methylenetetrahydrofolate reductase gene mutation

Ibrahim PİSKİN 1, Makbule ERCAN 2 , Nazmiye YÜKSEK 3, Ertug TOROSLU 1, Zuhal ORNEK 1

1 Department of Pediatrics, Faculty of Medicine, Bülent Ecevit University, Zonguldak, Turkey; 2 Department of Pediatrics, Alaca Public Hospital, Çorum, Turkey; 3 Division of Pediatric Hematology-Oncology, Department of Pediatrics, Faculty of Medicine, Bülent Ecevit University, Zonguldak, Turkey


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Publication History

Issue published online: June 7, 2017
Manuscript accepted: January 4, 2016
Manuscript revised: October 29, 2015
Manuscript received: August 19, 2015

Cite this article as

Piskin I, Ercan M, Yüksek N, Toroslu E, Ornek Z. Purpura Fulminans as the presenting manifestation in a patient with homozygous methylenetetrahydrofolate reductase gene mutation. Minerva Pediatr 2017;69:370-2. DOI: 10.23736/S0026-4946.16.04434-X

Corresponding author e-mail

cevik_ercan_@hotmail.com