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Pachyonychia Congenita - Can a Specific Phenotype be a Clue to a Genetic Defect? - a Case Report and Literature Review Cover

Pachyonychia Congenita - Can a Specific Phenotype be a Clue to a Genetic Defect? - a Case Report and Literature Review

Serbian Journal of Dermatology and Venereology
Volume 9 (2017): Issue 3 (September 2017)
By: Jovan Lalošević,  Mirjana Gajić-Veljić,  Jelena Stojković-Filipović,  Martina Bosić and  Miloš Nikolić  
Open Access
|Mar 2018

Authors

Jovan Lalošević

drjovanlalosevic@gmail.com

Clinic of Dermatovenereology, Clinical Center of Serbia, Belgrade, Serbia

Mirjana Gajić-Veljić

Clinic of Dermatovenereology, Clinical Center of Serbia, Belgrade, Serbia
University of Belgrade, School of Medicine, Belgrade, Serbia

Jelena Stojković-Filipović

Clinic of Dermatovenereology, Clinical Center of Serbia, Belgrade, Serbia
University of Belgrade, School of Medicine, Belgrade, Serbia

Martina Bosić

University of Belgrade, School of Medicine, Belgrade, Serbia

Miloš Nikolić

Clinic of Dermatovenereology, Clinical Center of Serbia, Belgrade, Serbia
University of Belgrade, School of Medicine, Belgrade, Serbia
DOI: https://doi.org/10.1515/sjdv-2017-0012 | Journal eISSN: 2406-0631
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Language: English
Page range: 119 - 123
Published on: Mar 24, 2018
Published by: Serbian Association of Dermatovenereologists (SAD)
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
Keywords:
Pachyonychia Congenita,
Child,
Signs and Symptoms,
Skin Diseases,
Genetic,
Mutation,
Phenotype,
Case Reports
Related subjects:
Medicine,
Clinical medicine,
Dermatological and veneral diseases

© 2018 Jovan Lalošević, Mirjana Gajić-Veljić, Jelena Stojković-Filipović, Martina Bosić, Miloš Nikolić, published by Serbian Association of Dermatovenereologists (SAD)
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

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