Results 71 to 80 of about 46,445 (154)

Pachydermoperiostosis (Touraine–Solente–Gole syndrome): a case report

open access: yesJournal 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

Table1_Etoricoxib as a treatment of choice for patients with SLCO2A1 mutation exhibiting autosomal recessive primary hypertrophic osteoarthropathy: A case report.docx

open access: yes, 2022
We reported a 22-year-old Emirati male with autosomal recessive primary hypertrophic osteoarthropathy caused by a possibly pathogenic homozygous non-synonymous variant in the SLCO2A1 gene (NM_005630.3: c.289C>T, p.
Nadia Akawi (3461522)   +4 more
core   +1 more source

Resolution of Thyroid Acropachy in a Patient Treated With Teprotumumab: A Case Report and Review of Mechanisms

open access: yesCase Reports in Endocrinology, Volume 2025, Issue 1, 2025.
Graves’ disease is an autoimmune thyroidopathy associated with hyperthyroidism and nonendocrine manifestations such as thyroid eye disease (TED), pretibial myxedema, and thyroid acropachy. Thyroid acropachy is an uncommon but debilitating condition, typically characterized by digital clubbing, soft tissue swelling, and periosteal new bone formation in ...
Soumya Chatterjee, Toshihiro Kita
wiley   +1 more source

Hypertrophic Pulmonary Osteoarthropathy Associated with Primary Adenocarcinoma of the Lung [PDF]

open access: yes, 1991
Hypertrophic pulmonary osteoarthropathy (HPOA) associated with primary lung cancer is reported in a fifty-four-year-old man. Symptoms of HPOA were makedly improved following lung resection for adenocarcinoma of the lung.Acta medica Nagasakiensia.
Tsuji, Hiroharu   +7 more
core   +1 more source

Exome Sequencing Identifies SLCO2A1 Mutations as a Cause of Primary Hypertrophic Osteoarthropathy [PDF]

open access: yes, 2012
By using whole-exome sequencing, we identified a homozygous guanine-to-adenine transition at the invariant −1 position of the acceptor site of intron 1 (c.97−1G>A) in solute carrier organic anion transporter family member 2A1 (SLCO2A1), which encodes a ...
Yue, Hua   +13 more
core   +1 more source

Detection and Molecular Characterization of 9000-Year-Old Mycobacterium tuberculosis from a Neolithic Settlement in the Eastern Mediterranean [PDF]

open access: yes, 2008
Background: Mycobacterium tuberculosis is the principal etiologic agent of human tuberculosis. It has no environmental reservoir and is believed to have co-evolved with its host over millennia.
Eshed Vered   +39 more
core   +1 more source

Hypertrophic osteoarthropathy in a child with biliary atresia.

open access: yes, 2004
Hypertrophic osteoarthropathy is a syndrome characterized by clubbing of the digits of the hand/foot, periosteal reaction and arthralgia or arthritis which is usually secondary to cyanotic congenital heart disease and chronic pulmonary infections. This
Kansu Tanca, Aydan
core  

Hypertrophic cardiomyopathy and ultra-endurance running - two incompatible entities? [PDF]

open access: yes, 2011
Regular and prolonged exercise is associated with increased left ventricular wall thickness that can overlap with hypertrophic cardiomyopathy (HCM). Differentiating physiological from pathological hypertrophy has important implications, since HCM is the ...
Sanjay K Prasad   +23 more
core   +1 more source

Pachydermoperiostosis ('Touraine-Solente-Gole' Syndrome)

open access: yesNepal 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
doaj   +3 more sources

Touraine–Solente–Gole syndrome: Clinical manifestation with bilateral true eyelid ptosis

open access: yesJPRAS Open, 2019
Touraine–Solente–Gole syndrome (pachydermoperiostosis [PDP] or primary idiopathic hypertrophic osteoarthropathy [HOA]) is a rare hereditary disorder that is characterized by a triad of manifestations that consists of skin changes (pachydermia), abnormal ...
Nutthawut Akaranuchat   +1 more
doaj   +1 more source

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