A Complete Form of Pachydermoperiostosis Accompanied by a Pituitary Microadenoma

Pachydermoperiostosis is a rare genetic disease that is associated with HPGD (15-hydroxyprostaglandin dehydrogenase) and SLCO2A1 (solute carrier organic anion transporter family member 2A1) gene mutations. It is characterized by three major phenotypes, namely, pachydermia, periostosis, and digital c...

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Detalles Bibliográficos
Autores principales: Chen, Yan Jing, Li, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830955/
https://www.ncbi.nlm.nih.gov/pubmed/36636633
http://dx.doi.org/10.2147/CCID.S389766

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830955/
https://www.ncbi.nlm.nih.gov/pubmed/36636633
http://dx.doi.org/10.2147/CCID.S389766

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