[HTML][HTML] Identification of the mutations in the prostaglandin transporter gene, SLCO2A1 and clinical characterization in Korean patients with pachydermoperiostosis

S Lee, SY Park, HJ Kwon, CH Lee… - Journal of Korean …, 2016 - ncbi.nlm.nih.gov
Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy, is a rare genetic
disease affecting both skin and bones. Both autosomal dominant with incomplete …

A case of pachydermoperiostosis treated by oral administration of a bisphosphonate and arthroscopic synovectomy

H Jojima, K Kinoshita, M Naito - Modern rheumatology, 2007 - academic.oup.com
Pachydermoperiostosis (PDP) is a rare hereditary disorder characterized by pachydermia,
digital clubbing, and periosteal hypertrophy. Here, we report a case of PDP showing …

Three-phase skeletal scintigraphy in pachydermoperiostosis

S Santhosh, A Bhattacharya, S Bhadada… - Clinical Nuclear …, 2011 - journals.lww.com
Pachydermoperiostosis or primary hypertrophic osteoarthropathy is a rare syndrome with
diverse radiologic and clinical features. Though the diagnosis can be made on the basis of …

[HTML][HTML] Incomplete form of Primary Hypertrophic Osteoarthropathy (Touraine-Solente-Gole Syndrome) Masquerading as Polyartrhalgia Diagnosed in Technetium …

T Sivathapandi, J Amalachandran… - Indian Journal of …, 2018 - journals.lww.com
The primary hypertrophic osteoarthropathy (PHOA)(pachydermoperiostosis) is a rare
genetic/hereditary disease characterized by skin changes (pachydermia), clubbing of fingers …

[HTML][HTML] Tc-99m MDP bone scintigraphy in a case of Touraine-Solente-Gole syndrome

R Mudalsha, MJ Jacob, C Jora… - Indian Journal of Nuclear …, 2011 - journals.lww.com
Pachydermoperiostosis is a form of primary hypertrophic osteoarthropathy, also known as
Touraine-Solente-Gole syndrome. It is a rare disease. In this report, we present the case of a …

Hypertrophic osteoarthropathy in a patient with primary hepatic angiosarcoma

J Zhang, M Dong, Z Yi, C Yu - Clinical Nuclear Medicine, 2020 - journals.lww.com
Primary hepatic angiosarcoma was diagnosed in a 59-year-old woman who presented an
arthralgia of limbs and dry cough for 6 weeks. Physical examination revealed digital …

[PDF][PDF] Pachydermoperiostosis (primary hypertrophic osteoarthropathy): case report

MH Paik, BY Lee, KH Lee, KS Song, JW Kim… - Journal of the Korean …, 2002 - jksronline.org
We report a case involving a young male with the complete form of primary hypertrophic
osteoarthropathy. He presented with the typical features of the condition: thickening and …

PP18. A case series of chronic non-bacterial osteomyelitis

A Islam, S Qasim, T Amin, M Wood, V Leone - Rheumatology, 2015 - academic.oup.com
Background: Primary hypertrophic osteoarthropathy (PHOA1) is a rare genetic condition
caused by mutation of the hydroxyprostaglandin dehydrogenase (HDPG) gene leading to …

原发性厚皮性骨膜增生症骨显像一例

解朋, 黄建敏, 张芳, 刘晓梅, 傅鹏, 高建青… - 中华核医学与分子影像 …, 2016 - cqvip.com
原发性厚皮性骨膜增生症骨显像一例-[维普官方网站]-www.cqvip.com-维普网 我的维普 购物车
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[CITATION][C] Arthritis & Allied Conditions 15th Edition

RD Altman