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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Dove
2023
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| 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 |