Back to search

Article

Complete Form of Pachydermoperiostosis with Good Initial Response to Etoricoxib: A Case Report

2022-11-21

Abstract excerpt

Pachydermoperiostosis (PDP) is a rare genetic disorder with unclear etiopathogenesis. We report a case of a 38-years-old male who presented with classic features of PDP. Patient showed a good initial response to Etoricoxib therapy but the safety and efficacy over long-term use are yet to be determined in further studies.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
a46ef5ce-063f-5afc-80e3-3a189620cd3e
DOI
10.22541/au.166902314.44960904/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Complete Form of Pachydermoperiostosis with Good Initial Response to Etoricoxib: A Case ReportDOI 10.22541/au.166902314.44960904/v1
A case of complete form of pachydermoperiostosis with SLCO2A1 mutations.Semantic proximity
Complete form of pachydermoperiostosis with SLCO2A1 gene mutation in a Korean family.Semantic proximity
Successful treatment of pachydermoperiostosis with etoricoxib in a patient with a homozygous splice-site mutation in the SLCO2A1 gene.Semantic proximity
Complete type of pachydermoperiostosis with a novel mutation c.510G>A of the SLCO2A1 gene.Semantic proximity
Pachydermoperiostosis in an African patient caused by a Chinese/Japanese SLCO2A1 mutation-case report and review of literature.Semantic proximity
Complete form of pachydermoperiostosis: a case report.Semantic proximity
Case of pachydermoperiostosis with solute carrier organic anion transporter family, member 2A1 (SLCO2A1) mutations.Semantic proximity
Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis.Semantic proximity
Pachydermoperiostosis: an update.Semantic proximity
The complete type of pachydermoperiostosis: a novel nonsense mutation p.E141* of the SLCO2A1 gene.Semantic proximity
Pachydermoperiostosis.Semantic proximity
Pachydermoperiostosis: The value of molecular diagnosis.Semantic proximity
Select a neighboring publication to make it the new centre.