Results 21 to 30 of about 808 (216)
Bilateral Ptosis Due to a Rare Cause-Pachydermoperiostosis [PDF]
Pachydermoperiostosis is a rare hereditary disorder that is characterised by pachydermia (thickening of the facial skin and/ or scalp), and periostosis (swelling of the periarticular tissue and a subperiosteal new bone formation).
Mahesh M, K V K S N Murthy
doaj +1 more source
Complete form of pachydermoperiostosis, [PDF]
Pachydermoperiostosis (PDP) or primary hypertrophic osteoarthropathy (PHO) is a rare hereditary disease characterized by digital clubbing, pachydermia, and periostosis. Its pathogenesis is uncertain and the diagnosis is based on clinical and radiological
Mônica Larissa Padilha Honório +2 more
doaj +1 more source
Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report
X‐ray of hand showing cortical thickening and periosteal reaction in distal radius ulna and phalynges of hand of a patient with pachydermoperiostosis. Key Clinical Message Pachydermoperiostosis is a rare genetic disorder that closely resembles acromegaly. Diagnosis is usually based on distinct clinical and radiological features. Oral etoricoxib therapy
Abinash Baniya +6 more
wiley +1 more source
Paraneoplastic syndrome of arthropathies as presenting sign for non‐small cell lung cancer
The aim of this study is to showcase an example of paraneoplastic syndrome, so other healthcare providers can be aware of early NSCLC manifestations. This is also important so providers do not dismiss review of symptoms that may not seem pertinent. Abstract The aim of this study is to showcase an example of paraneoplastic syndrome, so other healthcare ...
Alexander Kyle Lee +2 more
wiley +1 more source
Atypical Femoral Fracture in Hypophosphatasia: A Systematic Review
Objective. To summarize the characteristics of all reported patients with hypophosphatasia (HPP) who sustained atypical femoral fracture (AFF) and identify all available evidence to quantify the rate of coexistence between HPP and AFF. Methods. Potentially eligible articles were identified from the MEDLINE and EMBASE databases from its inception to ...
Nipith Charoenngam +7 more
wiley +1 more source
Missing data in bioarchaeology II: A test of ordinal and continuous data imputation
Abstract Objectives Previous research has shown that while missing data are common in bioarchaeological studies, they are seldom handled using statistically rigorous methods. The primary objective of this article is to evaluate the ability of imputation to manage missing data and encourage the use of advanced statistical methods in bioarchaeology and ...
Amanda Wissler +2 more
wiley +1 more source
Abstract Roman Macedonia has been largely neglected by bioarcheological research. As a result, little is known about the imprint of living conditions of that time on the skeletons of its inhabitants, especially those of the lower classes. This paper presents the paleopathological study conducted on a Roman period (1st–4th c.
Chryssa Vergidou +3 more
wiley +1 more source
The pedicle screw retractor can be temporarily installed on unilateral pedicle screws to provide traction to expand the intervertebral space, allowing for more operation space and nerve protection for transforaminal lumbar interbody fusion (TLIF). Furthermore, the retractor had the capacity to maintain the disc height achieved by paddle distractors ...
Hongwei Xie, Ziyu Ouyang, Hua Zhang
wiley +1 more source
Identifying treponemal disease in early East Asia
Syphilis in China before Vasco da Gama? Abstract Objectives Historic records suggest that a virulent form of treponematosis, sexually transmitted syphilis was introduced to Asia from Europe by the da Gama crew, who landed in India in 1498. Our objective is to assess the gross pathology of human skeletal remains from the Tang dynasty of China to test ...
Yawei Zhou +8 more
wiley +1 more source
Touraine-Solente-Gole Syndrome: A Rare Case Report
Touraine-Solente-Gole Syndrome, also known as Pachydermoperiostosis (PDP) or Primary Hypertrophic Osteoarthropathy, is a rare hereditary disorder, which affects both bones and skin.
Dharmil Doshi +2 more
doaj +1 more source

