Results 91 to 100 of about 2,048 (238)
Complete pachydermoperiostosis: A case report
Electronic Journal of General MedicinePachydermoperiostosis (PDP), also known as Touraine-Solente-Gole syndrome or primary hypertrophic osteoarthropathy, is a very rare disease mainly characterized by pachyderma, finger clubbing, hyperhidrosis, and periostosis.
Mohd Firdaus Abdul Mubing +3 more
semanticscholar +1 more source
The psoriatic great toe or the psoriatic onycho-pachydermo-periostitis of great toe (OP3gt) [PDF]
, 2011 The onycho-pachydermo-periostitis of the great toe is a characteristic feature of psoriatic arthritis first described by Fournie in 1980. In the affected patients, the great toe involvement is characterised by a relevant osteo-periostitis of the distal ...
C. Contessa +3 more
core +2 more sources
Cutis verticis gyrata resection with scalp reconstruction: a case report [PDF]
, 2023 Cutis verticis gyrata is a disease characterized by hypertrophy of the skin on the scalp, leading to the formation of folds and sacculations that resemble the gyrus of the cerebral cortex. It most commonly affects males and develops after puberty. It can
Augusto Massaud Pedretti +4 more
core +1 more source
Biologics for inherited disorders of keratinisation: A systematic review
Australasian Journal of Dermatology, Volume 65, Issue 2, Page 185-214, March 2024.Abstract Background/Objectives Recent literature highlights the potential of biologics in the management of inherited disorders of keratinisation. In this study, we conducted a systematic review of existing literature on treatment outcomes of inherited keratinisation disorders treated with biologics.
Michelle K. Y. Chen +3 more
wiley +1 more source
Pachydermoperiostosis: The Elephant Skin Disease [PDF]
The Journal of Rheumatology, 2017 Pachydermoperiostosis (PDP) was first described in 1868. Three forms have been identified: complete (clubbing, periostosis, pachyderma, and cutis verticis gyrata), incomplete (without cutis verticis gyrata), and forme fruste (pachyderma with minimal skeletal changes)1. Two genes have been associated, HPGD and SLCO2A1 2. A 27-year-old British Pakistani
Amidevi Desai +4 more
openaire +3 more sources
United European Gastroenterology Journal, Volume 12, Issue 1, Page 1-4, February 2024.JEADV Clinical Practice, Volume 4, Issue 1, Page 1-6, March 2025.
wiley +2 more sources
Involvement of DKK1 secreted from adipose‐derived stem cells in alopecia areata
Cell Proliferation, Volume 57, Issue 3, March 2024.IFNγ stimulates an increase in DKK1 levels in adipose‐derived stem cells (ASCs) through the activation of the STAT3 pathway. The secreted DKK1 promotes inflammation and inhibits follicular growth. However, when DKK1 is knocked out in ASCs, it deactivates the NF‐kB pathway, resulting in reduced cytokine levels and suppression of the inflammatory ...
Nahyun Choi +5 more
wiley +1 more source
Bone Research Society 2021 Abstracts
, 2021 JBMR Plus, Volume 5, Issue S5, November 2021.
wiley +1 more source
Pachydermoperiostosis (idiopathic hypertrophic osteoarthropathy) [PDF]
Postgraduate Medical Journal, 1981 Summary A Chinese patient with the incomplete form of pachydermoperiostosis is described. Brief comments on the diagnosis, familial occurrence and management are given.
Y. L. Yu, W. P. G. Turck
openaire +3 more sources
A Case of Elephant Extremities in a Filipino Male: Primary Familial Pachydermoperiostosis
Acta medica Philippina, 2022 This is a rare case of primary pachydermoperiostosis (PDP). A 28-year-old Filipino male presented with a lifelong history of enlarged hands and feet. He eventually developed symmetrical swelling of the ankles and knees associated with leg heaviness and ...
Geraldine T. Zamora-Abrahan +4 more
semanticscholar +1 more source