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Serbian Journal of Dermatology and Venereology
Volume 9 (2017): Issue 3 (September 2017)
Open Access
Pachyonychia Congenita - Can a Specific Phenotype be a Clue to a Genetic Defect? - a Case Report and Literature Review
Jovan Lalošević
Jovan Lalošević
,
Mirjana Gajić-Veljić
Mirjana Gajić-Veljić
,
Jelena Stojković-Filipović
Jelena Stojković-Filipović
,
Martina Bosić
Martina Bosić
and
Miloš Nikolić
Miloš Nikolić
| Mar 24, 2018
Serbian Journal of Dermatology and Venereology
Volume 9 (2017): Issue 3 (September 2017)
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Published Online:
Mar 24, 2018
Page range:
119 - 123
DOI:
https://doi.org/10.1515/sjdv-2017-0012
Keywords
Pachyonychia Congenita
,
Child
,
Signs and Symptoms
,
Skin Diseases
,
Genetic
,
Mutation
,
Phenotype
,
Case Reports
© 2017 Jovan Lalošević et al., published by De Gruyter Open
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.
Jovan Lalošević
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