Results 201 to 210 of about 91,488 (232)
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Primary hypertrophic osteoarthropathy

Seminars in Arthritis and Rheumatism, 1988
We describe seven patients with primary HOA and review 125 cases reported in the English, French, and German literature. The salient clinical features of primary HOA are: a bimodal distribution of disease onset with one peak during the first year of life and the other at age 15, a male predominance (nine to one), uncommon benign joint effusion, and a ...
M, Martínez-Lavín   +6 more
openaire   +2 more sources

Idiopathic hypertrophic osteoarthropathy

The Indian Journal of Pediatrics, 1980
A case of idiopathic hypertrophic osteo-arthropathy without pachydermia, in an 8-year-old boy born of non-consanguineous parents is described, with a brief review of the literature.
M, Purohit, S, Saxena, A, Garg
openaire   +2 more sources

Hypertrophic Pulmonary Osteoarthropathy

Diseases of the Chest, 1967
The records of 1,888 cases of pulmonary neoplasm operated on at the Mayo Clinic between 1953 and 1963 were reviewed. The incidence of hypertrophic pulmonary osteoarthropathy for the total group of cases, including both benign and malignant primary lung tumors as well as tumors metastatic to the lung, was 9.2 per cent.
J H, Stenseth   +2 more
openaire   +2 more sources

DISAPPEARING HYPERTROPHIC OSTEOARTHROPATHY

Rheumatology, 1988
A case is presented in which florid hypertrophic osteoarthropathy regressed clinically and radiologically when a Celestin tube was removed.
I, Haslock, V, Vasanthakumar
openaire   +2 more sources

Primary hypertrophic osteoarthropathy

Pediatric Radiology, 1986
In this article a family with five members suffering from primary hypertrophic osteoarthropathy (PHO) is reported. Our cases are characterized by swollen and painful joints and clubbing of distal phalanges of hands and feet. The diagnosis made upon on radiological and clinical findings.
H B, Diren   +5 more
openaire   +2 more sources

Primary hypertrophic osteoarthropathy

Rheumatology International, 2010
Pachydermoperiostosis PDP (idiopathic or primary hypertrophic osteoarthropathy) is a rare congenital disease that inherited in an autosomal fashion. The disease is more common in males and develops gradually from adulthood. The disease is characterized by coarse facial features, clubbing of the fingers and radiographic periostitis of the distal long ...
Hadi, Poormoghim   +2 more
openaire   +2 more sources

Digital clubbing as the predominant manifestation of hypertrophic osteoarthropathy caused by pathogenic variants in HPGD in three Indian families

Clinical Dysmorphology, 2020
Supplemental Digital Content is available in the text. 15-Hydroxyprostaglandin dehydrogenase is NAD+-dependent catalytic enzyme involved in prostaglandin biosynthesis pathway encoded by HPGD.
P. Radhakrishnan   +6 more
semanticscholar   +1 more source

Hypertrophic Osteoarthropathy and Pregnancy

Annals of Internal Medicine, 1969
Abstract Two patients developed hypertrophic osteoarthropathy during pregnancy. Both had immediate cessation of symptoms after delivery.
E C, Borden, H E, Holling
openaire   +2 more sources

Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of SLCO2A1

Modern Rheumatology Case Reports, 2020
Male, 41 years old (yo) had been complaining of severe arthralgia. Past History indicated obstruction of intestinal tract at 12 yo and gastric ulcer at 13 yo.
T. Ishizuka   +9 more
semanticscholar   +1 more source

Diagnosis and Management of a Patient With Primary Hypertrophic Osteoarthropathy With SCLO2A1 Pathogenic Variants in Vietnam.

Journal of clinical rheumatology, 2020
A 19-year-old male patient came to our attention with multiple prior hospital visits because of swelling of the hands and knees, decreased hand mobility, and frequent fatigue. The initial diagnosis of this patient was rheumatoid arthritis.
T. Tran   +9 more
semanticscholar   +1 more source

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