The first case of primary hypertrophic osteoarthropathy with soft tissue giant tumors caused by HPGD loss-of-function mutation

Background: Primary hypertrophic osteoarthropathy (PHO) is a rare genetic multi-organic disease characterized by digital clubbing, periostosis and pachydermia. Two genes, HPGD and SLCO2A1, which encodes 15-hydroxyprostaglandin dehydrogenase (15-PGDH) and prostaglandin transporter (PGT), respectively...

Olles dieđut

Bibliográfalaš dieđut

Váldodahkkit:	Qianqian Pang, Yuping Xu, Xuan Qi, Yan Jiang, Ou Wang, Mei Li, Xiaoping Xing, Ling Qin, Weibo Xia
Materiálatiipa:	Artigo
Giella:	Inglês
Almmustuhtton:	Bioscientifica 2019-06-01
Ráidu:	Endocrine Connections
Fáttát:	primary hypertrophic osteoarthropathy PHO HPGD mutation soft tumor COX2 selective inhibitor treatment
Liŋkkat:	https://ec.bioscientifica.com/view/journals/ec/8/6/EC-19-0149.xml
Fáddágilkorat:	Lasit fáddágilkoriid Eai fáddágilkorat, Lasit vuosttaš fáddágilkora!