Results 51 to 60 of about 2,048 (238)

Pachydermoperiostosis mimicking the acral abnormalities of acromegaly [PDF]

Endocrine, 2020
Collier, D, Korbonits, M, Marques, P, Stelmachowska-Banas, M, Wernig, F   +4 more
core   +2 more sources

Rhytidectomy for pachydermoperiostosis

Indian Journal of Dermatology, Venereology and Leprology, 2021
Neha Taneja, D R Gunaabalaji, Somesh Gupta   +2 more
openaire   +5 more sources

Bilateral Ptosis Due to a Rare Cause-Pachydermoperiostosis [PDF]

Journal of Clinical and Diagnostic Research, 2013
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

Case report: Schizophrenia and hypertrophic osteoarthropathy, a rare syndrome hiding a life‐threatening condition

Clinical Case Reports, Volume 10, Issue 1, January 2022., 2022
Schizophrenia is associated to somatic diseases. We describe an association with hypertrophic osteoarthropathy (HPO). It is a rare clinical entity but it could be a paraneoplastic syndrome hiding a life‐threatening condition. Abstract Schizophrenia is associated to somatic disorders especially cardio‐vascular and auto‐immune.
Emna Baklouti, Mehdi Karoui, Rania Kammoun, Faten Ellouze   +3 more
wiley   +1 more source

Coexistence of Touraine-Solente-Gole syndrome and type 1 neurofibromatosis: A case report

Turkderm Turkish Archives of Dermatology and Venereology, 2021
Pachydermoperiostosis is a rare syndrome that affects the skin and skeletal system. Mutations in the gene encoding hydroxyprostaglandin dehydrogenase (HPGD) are thought to play a role in disease etiopathogenesis.
Selma Korkmaz, Hakan Korkmaz, İjlal Erturan, Havva Hilal Ayvaz, Kuyaş Hekimler Öztürk, Mehmet Yıldırım   +5 more
doaj   +1 more source

A Rare Cause of Refractory Anaemia hidden between Folds

, 2023
British Journal of Haematology, Volume 202, Issue 4, Page 712-712, August 2023.
Syna Hamani, Bruno Lioure, Alina Nicolae, Dan Lipsker   +3 more
wiley   +1 more source

Pachydermoperiostosis – Mimic to acromegaly [PDF]

Medical Journal Armed Forces India, 2015
Hypertrophic osteoarthropathy (HOA) is a clinical syndrome that causes clubbing of the fingers and toes, enlargement of the extremities and pain and swelling of the joints. Patients may have one or more of these manifestations. The syndrome can be primary or secondary.
M.L. Sharma, Yashpal Singh, M.K. Garg, S. Mishra   +3 more
openaire   +3 more sources

Pachydermoperiostosis in a patient with chronic hepatitis B virus infection referred as acromegaly: a case report

Journal of Medical Case Reports, 2018
Background Primary hypertrophic osteoarthropathy also known as pachydermoperiostosis is a rare genetic disorder that has often been confused with acromegaly because of similar clinical features.
Yacoba Atiase, Ernest Yorke, Josephine Akpalu, Bismark Opoku-Asare, Patrick Adjei, Maame Boatemma Amissah-Arthur, Albert Akpalu   +6 more
doaj   +1 more source

Features of the clinical course of pachydermoperiostosis with a verified mutation in the European type gene

Osteoporosis and Bone Diseases, 2023
Pachydermoperiostosis (primary hypertrophic osteoarthropathy) is an orphan disease, the main clinical manifestations of which include pin-shaped deformity of the fingers according to the type of «drumsticks», periostosis (non-inflammatory changes of the ...
T. M. Frolova, O. Golounina, E. Mamedova, E. E. Litvinova, Z. Belaya   +4 more
semanticscholar   +1 more source

5 Cases Analysis of Pachydermoperiostosis Complicated with Synovitis

罕见病研究, 2023
Objective To analyze the clinical characteristics, treatments and prognosis of pachydermoperiostosis (PDP) with synovitis, and to improve clinicians′ understanding of PDP. Methods The clinical data of 5 patients diagnosed with PDP in Peking Union Medical
LU Xin, YANG Bo, ZHANG Jianguo
doaj   +1 more source