Results 61 to 70 of about 2,284 (209)
Pediatric Rheumatology Online Journal, 2023 Background Primary Hypertrophic Osteoarthropathy (PHO), also known as Touraine-Solente-Gole Syndrome, is a rare, multisystemic autosomal recessive disorder caused by pathogenic variants in the 15-hydroxyprostaglandin dehydrogenase (HPGD) or Solute ...
Rafaela Nicolau +7 more
doaj +1 more source
Osteoartropatia hipertrófica associada a linfoepitelioma de nasofaringe: relato de caso [PDF]
, 2012 Malignant neoplasms of the nasopharynx are very rare and has two peaks of incidence: below the age of 30, and between the 4th and 5th decade of life. It is, however, uncommon after the 60 years of age.
Cotrim, Deborah P. +1 more
core +2 more sources
Animal models of tendon calcification: Past, present, and future
Animal Models and Experimental Medicine, Volume 7, Issue 4, Page 471-483, August 2024.Various modeling methods for experimental animal models of tendon calcification are shown in the figure: the methods of modeling tendon calcification in experimental animals as shown in the figure can be mainly classified as trauma induced, tissue factor injections, dietary or pharmacological modifications, and gene knockouts.
Ruichen Li +8 more
wiley +1 more source
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 +2 more
wiley +1 more source
Tuberculosis in Retrospective: Review of Current Knowledge and its Application in the Study of Skeletal Remains [PDF]
, 2012 La tuberculosis fue en el pasado, al igual que en la actualidad, una enfermedad con una alta morbilidad y mortalidad. Sin embargo, su detección en el registro arqueológico humano es relativamente infrecuente.
Santos, Ana Luisa, Suby, Jorge Alejandro
core
Solitary Fibrous Tumour of the Pleura and Paraneoplastic Symptoms:A Case Report and Literature Review [PDF]
, 2017 Background: Solitary Fibrous Tumors of the Pleura (SFTP) are rare neoplasms deriving from mesenchymal cells. They are mostly benign and may be accompanied by paraneoplastic syndromes, particularly hypoglycaemia and hypertrophic pulmonary osteoarthropathy
Braathen, Alexander, Bødtger, Uffe
core +1 more source
Influenza and Other Respiratory Viruses, Volume 18, Issue 3, March 2024.ABSTRACT Background Abnormal changes of monocytes have been observed in acute COVID‐19, whereas associations of monocyte count with long COVID were not sufficiently elucidated. Methods A cohort study was conducted among COVID‐19 survivors discharged from hospital. The primary outcomes were core symptoms of long COVID, distance walked in 6 min, and lung
Xiaoying Gu +9 more
wiley +1 more source
Pachydermoperiostosis (Touraine–Solente–Gole syndrome): a case report
Journal of Medical Case Reports, 2019 Background Pachydermoperiostosis (PDP) is a rare disorder characterized by clubbing of the fingers, thickening of the skin (pachyderma), and excessive sweating (hyperhidrosis).
Amir Joshi +4 more
doaj +1 more source
Molecular Genetics &Genomic Medicine, Volume 12, Issue 2, February 2024.Abstract Background Disease‐related variants in PHEX cause XLH by an increase of fibroblast growth factor 23 (FGF23) circulating levels, resulting in hypophosphatemia and 1,25(OH)2 vitamin D deficiency. XLH manifests in early life with rickets and persists in adulthood with osseous and extraosseous manifestations.
Maria Helena Vaisbich +10 more
wiley +1 more source
Reumatismo, 2013 Pachydermoperiostosis as the primary form of hypertrophic osteoarthropathy is a rare hereditary disorder with a number of characteristic findings, e.g. periosteal hypertrophy, digital clubbing and pachydermia.
S. Warwas +3 more
doaj +1 more source