Results 61 to 70 of about 729 (170)

Pseudoacromegaly—A challenging entity in the endocrine clinic: A systematic review

Clinical Endocrinology, Volume 100, Issue 6, Page 542-557, June 2024.
Abstract Objective Pseudoacromegaly encompasses conditions with features of acromegaly/gigantism, but no growth hormone (GH) or insulin‐like growth factor‐1 (IGF‐1) excess. We aimed to review published pseudoacromegaly cases evaluated due to clinical suspicion of acromegaly.
Pedro Marques, Inês Sapinho, Márta Korbonits   +2 more
wiley   +1 more source

Pachydermoperiostosis: a case report

Остеопороз и остеопатии, 2017
Pachydermoperiostosis (PHO) or primary hypertrophic osteoarthropathy is a rare genetic disease that typically begins during childhood or adolescence. It is characterized by digital clubbing, pachydermia and periosteal reaction and progresses gradually ...
Valentina A. Fursenko, Tatiana A. Grebennikova, Alexey G. Nikitin, Zhanna E. Belaya   +3 more
doaj   +1 more source

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, Juyeong Hwang, Doo Yeong Kim, Jino Kim, Seung Yong Song, Jong‐Hyuk Sung   +5 more
wiley   +1 more source

Clinical and Genetic Characteristics of Korean Patients Diagnosed with Chronic Enteropathy Associated with SLCO2A1 Gene: A KASID Multicenter Study

Gut and Liver, 2022
Background/Aims: Chronic enteropathy associated with SLCO2A1 gene (CEAS), an inherited disease characterized by nonspecific intestinal ulcers, has emerged in the Japanese population via loss-of-function mutations in the SLCO2A1 gene.
Hee Seung Hong, Jiwon Baek, Jae Chul Park, Ho-Su Lee, Dohoon Park, A-Ran Yoon, Soo Jung Park, Sung Noh Hong, Seong-Joon Koh, Chang Kyun Lee, Bo-In Lee, Sung Wook Hwang, Sang Hyoung Park, Seung-Jae Myung, Suk-Kyun Yang, Kyuyoung Song, Byong Duk Ye, on behalf of the IBD Research Group of the Korean Association for the Study of Intestinal Diseases   +17 more
doaj   +1 more source

Idiopathic hypertrophic osteoarthropathy misdiagnosed as juvenile idiopathic arthritis. Case study [PDF]

, 2023
Background. Pachydermoperiostosis (or primary hypertrophic osteoarthropathy) is a rare genetic disease that usually begins in childhood or adolescence, is characterized by certain clinical signs (pachydermia, periostosis, drum sticks) that gradually ...
Corotaș, Valeriu, Dutca, Lucia, Lucia Dutca, Popa, Serghei, Homițchi, Marinela, Marinela Homitchi, Svetlana Agachi, Agachi, Svetlana, Serghei Popa   +8 more
core   +1 more source

Form fruste pachydermoperiostosis associated with ptosis and floppy eyelid syndrome

, 2019
Pachydermoperiostosis (PDP), also known as idiopathic or primary hypertrophic osteoarthropathy or Touraine-Solente-Gole Syndrome, is a rare genetic disorder affecting skin and bone, consisting of pachydermia and periostosis.
Rubinov, Avi, Oryschak, Allan, Weis, Ezekiel, Bart, Bevin, Ting, Andrew   +4 more
core   +1 more source

Folded pachydermia associated with hair transplantation (case reports)

Folded pachydermia of the scalp is a rare benign condition characterized by skin hypertrophy and formation of pronounced folds. Despite the description of primary and secondary forms of the disease, an impact of surgical interventions — particularly hair
V.V. Gladko, G.A. Flaks, R.A. Pakhomova, A.A. Kolesnik, V.Ya. Kolesnik, V.A. Ivanova   +5 more
core   +1 more source

Acetaminophen as a possible safer alternative for reducing prostaglandin E2‐major urinary metabolites concentrations and alleviating joint pain in pachydermoperiostosis

JEADV Clinical Practice, Volume 4, Issue 1, Page 277-280, March 2025.
Tomoya Takegami, Takashi Nomura, Satoru Yonekura, Akiyoshi Senda, Kazue Yoshida, Atsuhito Seki, Kazuhiko Nakabayashi, Tadakazu Hisamatsu, Hiroki Kitamoto, Shuji Yamamoto, Yusuke Honzawa, Hiroshi Seno, Hironori Niizeki, Kenji Kabashima   +13 more
wiley   +1 more source

Pachydermoperiostosis And An Eyelid Ptosis Associated With Spiky Keratoderma – An Unusual Presentation

Nepal Journal of Dermatology, Venereology & Leprology, 2016
Pachydermoperiostosis, ( PDP), a rare hereditary disorder that is characterized by digital clubbing, pachydermia, subperiosteal new bone formation, associated with pain, polyarthritis, cutis verticis gyrata, seborrhoea and hyperhidrosis.
S Das, S Chakraborty, NS Sarkar
doaj   +3 more sources