Results 11 to 20 of about 3,467 (203)
Hypertrophic pulmonary osteoarthropathy is a rare paraneoplastic syndrome affecting
Takafumi Iguchi +4 more
doaj +2 more sources
Blepharoptosis and hypertrophic osteoarthropathy: A case report
A 52-year-old male patient presented to our hospital with a history of secondary hypertrophic osteoarthropathy (HOA) associated with an abdominal neoplasia and blepharoptosis. He had finger clubbing, hyperhidrosis, and hypertrichosis.
Aysun Sanal Dogan +2 more
doaj +2 more sources
Hypertrophic osteoarthropathy (HOA) is a condition characterized by aberrant skin and osseous tissue proliferation in the distal extremities. Mutations in the 15-hydroxyprostaglandin dehydrogenase gene (HPGD) and the soluble carrier organic anion carrier
Ilke Coskun Benlidayi +2 more
doaj +1 more source
Hypertrophic osteoarthropathy in a sheep [PDF]
: This research described the radiological, clinical and pathological aspects of hypertrophic osteoarthropathy in a seven-year-old Santa Inês ram. The main clinical features were lameness of the thoracic and pelvic limbs, rigid, cracking and enlarged of ...
Hisadora Advincula da Silva Chaves Bom +7 more
doaj +1 more source
Hypertrophic pulmonary osteoarthropathy secondary to pulmonary malignancy: A case report
Background: Hypertrophic pulmonary osteoarthropathy is a rare type of paraneoplastic rheumatic manifestation which classically presents with bilateral, symmetrical periostitis of long bones, digital clubbing, and non-inflammatory arthritic pain and ...
Steven R. Cooperman, Raffi Salibian
doaj +1 more source
Primary hypertrophic osteoarthropathy
The article presents information about a rare hereditary disease – primary hypertrophic osteoarthropathy with autosomal dominant and autosomal recessive inheritance.
E. L. Trisvetova
doaj +1 more source
Secondary Hypertrophic Osteoarthropathy
Chakraborty RK, Sharma S.
europepmc +3 more sources
Osteological and Biomolecular Evidence of a 7000-Year Old Case of Hypertrophic Pulmonary Osteopathy Secondary to Tuberculosis from Neolithic Hungary [PDF]
Seventy-one individuals from the late Neolithic population of the 7000-year-old site of Hódmezővásárhely-Gorzsa were examined for their skeletal palaeopathology.
Besra, Gurdyal S. +8 more
core +7 more sources
Pachydermoperiostosis (PDP) is a rare genodermatosis with prominent cutaneous, soft tissue and skeletal manifestations. It can mimic secondary causes of hypertrophic osteoarthropathy such as thyroid acropachy.
Ajani AA +5 more
doaj +1 more source

