Results 161 to 170 of about 1,595 (202)
Some of the next articles are maybe not open access.

Pachydermoperiostosis mimicking acromegaly: A case report

Journal of Association of Clinical Endocrinologist and Diabetologist of Bangladesh
Pachydermoperiostosis (PDP) is a rare clinical condition that is characterized by pachyderma (thickened facial skin), skeletal changes (periostosis), excessive sweating (hyperhidrosis), and acropachia (digital clubbing).
Md Ashiqur Rahman   +5 more
semanticscholar   +1 more source

Primary pachydermoperiostosis associated with pigmented villonodular synovitis: An unknown association?

International Journal of Rheumatic Diseases, 2023
Primary pachydermoperiostosis is a rare genetic disease affecting the skin and musculoskeletal system. In contrast to secondary hypertrophic osteoarthropathy, primary pachydermoperiostosis is considered a benign condition.
E. Rabhi   +6 more
semanticscholar   +1 more source

Acetaminophen as a possible treatment option for pachydermoperiostosis carrying mutated SLCO2A1: Case series

Journal of dermatology (Print)
Pachydermoperiostosis (PDP) is a genetic disease characterized by digital clubbing, periostosis, and pachydermia. PDP with these three features, along with cutis verticis gyrata (CVG), is categorized as the “complete form,” whereas cases without CVG are ...
T. Takegami   +8 more
semanticscholar   +1 more source

Pachydermoperiostosis.

The Journal of the Association of Physicians of India, 2018
A case of Pachydermoperiostosis (PDP) presented to us in rheumatology clinic with complaints of enlargement and broadening of bilateral hands and feet, grade IV digital clubbing, coarsening of facial features, excessive sweating of the palms, soles during summers.
Renu, Saigal   +5 more
openaire   +3 more sources

PSEUDOACROMEGALY IN A PATIENT WITH PACHYDERMOPERIOSTOSIS

Journal of the ASEAN Federation of Endocrine Societies
INTRODUCTION/BACKGROUNDPatients who are clinically suspected of acromegaly are usually referred to an endocrinologist. Biochemical evaluation is necessary to confirm the presence of an abnormality in the growth hormone (GH) axis.
Nur Husnina Matali   +3 more
semanticscholar   +1 more source

P19 A rare case of PHOAR2-enteropathy syndrome (PHOAR2E; previously known as pachydermoperiostosis) with a causal variant in the SLCO2A1 gene.

British Journal of Dermatology
We present a rare case of PHOAR2-enteropathy syndrome with a causal variant in the SLCO2A1 gene in an adolescent male who presented to the dermatology department for prominent deep creases on his forehead and fingers.
C. Grechin   +3 more
semanticscholar   +1 more source

Pachydermoperiostosis: an update

Clinical Genetics, 2005
Pachydermoperiostosis (PDP) is a rare genodermatosis, characterized by pachydermia, digital clubbing, periostosis and an excess of affected males. Although an autosomal dominant model with incomplete penetrance and variable expression has been proved, both autosomal recessive and X‐linked inheritance have been suggested.
M, Castori   +5 more
openaire   +2 more sources

Complete pachydermoperiostosis (Touraine–Solente–Gole Syndrome) in a young Yemeni man

Journal of Dermatology & Cosmetology
Pachydermoperiostosis (PDP) is a rare genodermatosis, caused by pathogenic variants in the 15-hydroxyprostaglandin dehydrogenase (HPGD) or Solute Carrier Organic Anion Transporter Family Member 2A1 (SLCO2A1) genes, affecting the skin and bones.
Mohammad Ali Alshamia   +2 more
semanticscholar   +1 more source

Pachydermoperiostosis: Cosmetic implications in a multi-system genetic condition.

Clincal and Experimental Dermatology
We present the case of a 17-year-old gentleman, initially referred to rheumatology with painful enlargement of his joints, along with prominence of facial features consistent with cutis verticis gyrata.
James W Dickens   +3 more
semanticscholar   +1 more source

Pachydermoperiostosis

Orbit, 2023
Md Shahid Alam, Shamayita Gupta
openaire   +2 more sources

Home - About - Disclaimer - Privacy