Results 21 to 30 of about 87,294 (214)

Characteristic Facial Appearance Was the Key to Diagnosing Chronic Enteropathy Associated with SLCO2A1-associated Primary Hypertrophic Osteoarthropathy. [PDF]

open access: yesIntern Med, 2020
Patients with chronic enteropathy associated with SLCO2A1 (CEAS) develop multiple circular, longitudinal, or eccentric ulcers in the ileum. It is sometimes difficult to distinguish CEAS from Crohn's disease. CEAS and primary hypertrophic osteoarthropathy
Sonoda A   +11 more
europepmc   +2 more sources

Primary hypertrophic osteoarthropathy related gastrointestinal complication has distinctive clinical and pathological characteristics: two cases report and review of the literature. [PDF]

open access: yesOrphanet J Rare Dis, 2019
BackgroundPrimary hypertrophic osteoarthropathy (PHO) is a rare disease related to HPGD and SLCO2A1 gene mutation. Gastrointestinal involvement of PHO is even rarer with unknown pathogenesis.
Wang Q   +7 more
europepmc   +2 more sources

HYPERTROPHIC PULMONARY OSTEOARTHROPATHY [PDF]

open access: bronzeThe Journal of Thoracic and Cardiovascular Surgery, 1963
Robert S. Brodey   +4 more
  +7 more sources

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

open access: yesEndocr Connect, 2019
Background Primary hypertrophic osteoarthropathy (PHO) is a rare genetic multi-organic disease characterized by digital clubbing, periostosis and pachydermia.
Pang Q   +8 more
europepmc   +2 more sources

Early Imaging Findings of Hypertrophic Osteoarthropathy Mimicking Bone Metastasis from Extrathoracic Malignancy [PDF]

open access: yes대한영상의학회지, 2021
Hypertrophic osteoarthropathy (HOA) is a syndrome characterized by digital clubbing, periosteal bone formation, and synovial effusions. Secondary HOA is associated with intrathoracic malignancy in most cases; however, in rare cases, HOA can be caused ...
Ji Yeon Hwang   +3 more
doaj   +2 more sources

Establishment of a novel human iPSC line (SDQLCHi032-A) derived from a patient with primary hypertrophic osteoarthropathy caused by HPGD homozygous mutation

open access: yesStem Cell Research, 2021
Primary hypertrophic osteoarthropathy, autosomal recessive type 1 (PHOAR1, MIM259100) is caused by mutations in the 15-hydroxyprostaglandin dehydrogenase gene (HPGD, MIM601688) on chromosome 4q34.
Yue Li   +8 more
doaj   +2 more sources

Hypertrophic pulmonary osteoarthropathy with primary lung cancer

open access: diamondMajalah Kedokteran Andalas, 2017
Hipertrophic Pulmonary Osteoarthropathy (HPO) merupakan sindrom paraneoplastik yang disebabkan oleh kelainan pada paru-paru. Angka kejadian HPO sangat rendah yaitu kurang dari 1%, dimana penyebab yang tersering (90%) adalah karsinoma bronkogenik ...
Yulia Kurniawati, A.H.S. Kartamihardja
doaj   +3 more sources

Blepharoptosis and hypertrophic osteoarthropathy: A case report

open access: yesIndian Journal of Ophthalmology, 2016
A 52-year-old male patient presented to our hospital with a history of secondary hypertrophic osteoarthropathy (HOA) associated with an abdominal neoplasia and blepharoptosis. He had finger clubbing, hyperhidrosis, and hypertrichosis.
Aysun Sanal Dogan   +2 more
doaj   +2 more sources

Incomplete form of Primary Hypertrophic Osteoarthropathy (Touraine-Solente-Gole Syndrome) Masquerading as Polyartrhalgia Diagnosed in Technetium-99m-Methylene Diphosphonate Scintigraphy: An Interesting Case Report

open access: greenIndian Journal of Nuclear Medicine, 2018
The primary hypertrophic osteoarthropathy (PHOA) (pachydermoperiostosis) is a rare genetic/hereditary disease characterized by skin changes (pachydermia), clubbing of fingers and periosteal thickening (periostitis) with sub-periosteal new bone formation.
Thangalakshmi Sivathapandi   +3 more
semanticscholar   +3 more sources

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