Pachydermoperiostosis ('Touraine-Solente-Gole' Syndrome)
Nepal Journal of Dermatology, Venereology & Leprology, 2013 DOI: http://dx.doi.org/10.3126/njdvl.v11i1.7937 Nepal Journal of Dermatology, Venereology & Leprology Vol.11(1) 2013 pp.64 ...
R Sharma +3 more
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A rare cause of digital clubbing: pachydermoperiostosis
The Pan African Medical Journal, 2016 A 35-year-old man of Tunisian origin complained of inflammatory arthralgia and he had noticed a progressive enlargement of his hands and feet as well as facial furrowing.
Zeineb Alaya, Walid Osman
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A case of finger clubbing associated with nasopharyngeal carcinoma in a young girl, and review of pathophysiology [PDF]
, 2009 Hypertrophic osteoarthropathy is characterized by clubbing of the digital tips and periosteal reaction of long bones. Most of the cases are associated with malignancy or other conditions such as congenital heart disease, liver cirrhosis, pulmonary ...
Abbasi, Ahmed Nadeem +5 more
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Pachydermoperiostosis or primary hypertrophic osteoarthropathy: A rare clinicoradiologic case
Indian Journal of Radiology and Imaging, 2009 Pachydermoperiostosis (PDP) or primary hypertrophic osteoarthropathy is a rare syndrome with diverse radiological and clinical features. Though the diagnosis can be made on the basis of the classic clinical and radiological features, it is often missed ...
Rajul Rastogi +5 more
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Imaging and reporting considerations for suspected physical abuse (non-accidental injury) in infants and young children. Part 2: axial skeleton and differential diagnoses [PDF]
, 2017 Recognising the skeletal manifestations of inflicted injury (II) in infants and young children is of crucial importance. There are specific fracture patterns which are highly suspicious of II in addition to common differential diagnoses with which ...
Offiah, A.C., Paddock, M., Sprigg, A.
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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
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
Vitiligo at Injection Site of PEG-IFN-α 2a in Two Patients with Chronic Hepatitis C: Case Report and Literature Review [PDF]
, 2010 A 72-year-old female and a 57-year-old male with chronic hepatitis C were treated with a combination therapy of pegylated interferon (PEG-IFN)-α 2a (180 μg s.c. once a week) and ribavirin (1,000 mg orally daily).
Arya, S. +4 more
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HYPERTROPHIC OSTEOARTHROPATHY IN A PATIENT WITH HETEROZYGOUS MUTATION IN THE SLCO2A1 GENE: A CASE REPORT [PDF]
, 2023 Hypertrophic osteoarthropathy (HOA) is a condition characterized by aberrant skin and osseous tissue proliferation in the distal extremities. Mutations in the 15-hydroxyprostaglandin dehydrogenase gene (HPGD) and the soluble carrier organic anion carrier
Ilke Coskun Benlidayi +2 more
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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