ReviewClinical rheumatology2012
Osteopoikilosis: what does the rheumatologist must know about it?
Review in Clinical rheumatology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
13 citing papers in PubMed, 42 citations in OpenAlex.
- Osteopoikilosis in a young ankylosing spondylitis patient.Journal of rheumatic diseases · 2024Article
- Article
- Review
- Result of cementless total hip arthroplasty in a patient with osteopoikilosis, hip dysplasia and advanced osteoarthritis: a case report.BMC musculoskeletal disorders · 2021Article
- Spotted bone disease.Clinical rheumatology · 2020Article
- Osteopoikilosis found incidentally in a 17-year-old adolescent with femoral shaft fracture: A case report.Medicine · 2017Article
- Identification of a novel LEMD3 Y871X mutation in a three-generation family with osteopoikilosis and review of the literature.Journal of endocrinological investigation · 2016Review
- Sclerosing bone dysplasias: genetic, clinical and radiology update of hereditary and non-hereditary disorders.The British journal of radiology · 2016Review
- Mutation in LEMD3 (Man1) Associated with Osteopoikilosis and Late-Onset Generalized Morphea: A New Buschke-Ollendorf Syndrome Variant.Case reports in dermatological medicine · 2016Article
- Osteopoikilosis: report of a familial case and review of the literature.Rheumatology international · 2015Review
- Osteopoikilosis: A rare cause of bone pain.Caspian journal of internal medicine · 2015Article
- Cystinosis with sclerotic bone lesions.JIMD reports · 2014Article
- Osteopoikilosis in the Mandible.Contemporary clinical dentistryArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Osteopoikilosis (OPK) is a rare, benign, and asymptomatic bone dysplasia that is developed during childhood and persists throughout life. This condition is generally found incidentally on plain radiographies made by other reasons. The main differential diagnosis is osteoblastic metastasis. So, OPK must be in differential diagnosis when bone lesions are identified on plain radiograph to avoid alarming the patient with more serious disease and misdiagnosis. In this paper, we review the clinical manifestation, pathophysiology, diagnosis, and treatment of OPK.
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Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.