Results 41 to 50 of about 4,323,847 (152)

Pachydermoperiostosis as a Rare Cause of Blepharoptosis

open access: yesTürk Oftalmoloji Dergisi, 2014
A 37-year-old male patient diagnosed with pachydermoperiostosis at another center came to our clinic to rectify his blepharoptosis. The physical examination of the patient revealed skeleton and skin symptoms typical for pachydermoperiostosis.
Özlem Yalçın Tök   +5 more
doaj   +1 more source

Hypertrophic Pulmonary Osteoarthropathy Associated with Primary Adenocarcinoma of the Lung [PDF]

open access: yes, 1991
Hypertrophic pulmonary osteoarthropathy (HPOA) associated with primary lung cancer is reported in a fifty-four-year-old man. Symptoms of HPOA were makedly improved following lung resection for adenocarcinoma of the lung.Acta medica Nagasakiensia.
Tsuji, Hiroharu   +7 more
core   +1 more source

Elevated Hemoglobin A2: A Molecular Revisited, and Implications to β‐Thalassemia Screening

open access: yesJournal of Clinical Laboratory Analysis, Volume 40, Issue 15, August 2026.
In Thailand, the Hb A2 cut‐off value for β‐thalassemia carrier has been changed from 4.0% to 3.6% since 2015. We examined the molecular basis of β‐thalassemia in a large cohort of Thai subjects with this change. The molecular basis of β‐thalassemia was updated, and a change in the Hb A2 cut‐off can alter this spectrum.
Kritsada Singha   +8 more
wiley   +1 more source

Pachydermoperiostosis-Like Disease In Captive Red Ruffled Lemurs (Varecia Variegatus Rubra) [PDF]

open access: yes, 2011
Pachydermatoperiostosis, a rare form of hypertrophic osteoarthropathy, is of unknown etiology and previously thought limited to humans. The only periosteal reaction previously reported in prosimians is related to renal disease.
Bruce Rothschild   +2 more
core  

Brainstem Tuberculous Abscess in a 63‐Year‐Old Adult With Unrepaired Tetralogy of Fallot

open access: yesCase Reports in Medicine, Volume 2026, Issue 1, 2026.
Background Tetralogy of Fallot (TOF) is a congenital heart anomaly usually corrected surgically in childhood. Reports of adults with unrepaired TOF indicate that they are at high risk of endocardial infections and sequelae such as distant abscesses. Case Presentation A 63‐year‐old man born and raised in Vietnam presented with unrepaired TOF and 5 days ...
Jessica S. Yang   +5 more
wiley   +1 more source

Hypertrophic osteoarthropathy in a child with nasopharyngeal carcinoma

open access: yes, 2000
We report a 13-year-old boy with nasopharyngeal carcinoma, skull metastases and hypertrophic osteoarthropathy, Although the metastases and the primary tumour responded well to chemotherapy, hypertrophic osteoarthropathy persisted during follow ...
Akyuz, C   +4 more
core   +1 more source

Table1_Etoricoxib as a treatment of choice for patients with SLCO2A1 mutation exhibiting autosomal recessive primary hypertrophic osteoarthropathy: A case report.docx

open access: yes, 2022
We reported a 22-year-old Emirati male with autosomal recessive primary hypertrophic osteoarthropathy caused by a possibly pathogenic homozygous non-synonymous variant in the SLCO2A1 gene (NM_005630.3: c.289C>T, p.
Nadia Akawi (3461522)   +4 more
core   +1 more source

Unexpected Link Between Myasthenia Gravis and Lung Adenocarcinoma: A Case Report

open access: yesCase Reports in Surgery, Volume 2026, Issue 1, 2026.
Introduction While myasthenia gravis (MG) is commonly associated with thymic abnormalities and other autoimmune diseases, its association with malignancies, particularly lung adenocarcinoma, is exceptionally rare. Case Presentation A 65‐year‐old male presented with bilateral eyelid drooping, double vision, and fatigable limb weakness, alongside a 4 ...
Biruke Temesgen   +6 more
wiley   +1 more source

Palmar Fasciitis and Polyarthritis With Erosive Disease: A Case Report

open access: yesCase Reports in Rheumatology, Volume 2026, Issue 1, 2026.
Palmar fasciitis and polyarthritis is a rare paraneoplastic syndrome that is nonerosive and associated with a high mortality rate. Metastatic undifferentiated epithelial carcinoma of unknown primary was diagnosed in a 59‐year‐old man who simultaneously developed palmar fasciitis and polyarthritis.
Zahraa Qamhieh   +2 more
wiley   +1 more source

Primary hypertrophic osteoarthropathy accompanied by Crohn's disease: a case report

open access: yes, 1997
Primary hypertrophic osteoarthropathy is a rare hereditary disease without evidence of underlying diseases. We report a very unusual case of primary HOA accompanied by Crohn's disease with the primary HOA mimicking secondary HOA, which is a rare ...
서진석
core   +1 more source

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