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pro vyhledávání: '"Caffey's disease"'
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Autor:
Martina Lari, Alessandra Modi, Chiara Vergata, Thomas Colard, Daniela Lombardo, Tristan Pascart, Annalisa Vetro, Benoit Bertrand, David Caramelli
Publikováno v:
International Journal of Osteoarchaeology. 29:854-859
Autor:
Sachin Khanduri, Aakshit Goyal, Tushar Sabharwal, Gaurav Katyal, Mriganki Chaudhary, Shreshtha Jain
Publikováno v:
Cureus
Caffey’s disease, also known as Infantile Cortical Hyperostosis, is a rare, self-limited, benign, inflammatory gene-related disorder of infants that causes bone changes, soft tissue swelling, and irritability. The mandible (75%), clavicles, and uln
Publikováno v:
Journal of the Belgian Society of Radiology; Vol 100, No 1 (2016); 10
Journal of the Belgian Society of Radiology
Journal of the Belgian Society of Radiology, Vol 100, Iss 1 (2016)
Journal of the Belgian Society of Radiology
Journal of the Belgian Society of Radiology, Vol 100, Iss 1 (2016)
to the Oncology Department of Hospital Pediatrico de Coimbra with a four day history of right facial swelling. Pain triggered by palpation was the only complaint. There was no effacement of the temporomandibular angle or palpable cervical lymphadenop
Publikováno v:
Irish Journal of Medical Science. 176:133-136
Caffey's disease or infantile cortical hyperostosis is a rare cause of irritability, bone pain, soft tissue swelling and fever in the infant.To review the presentation and diagnosis of an 8-week old infant with focal tenderness of the tibia.The sympt
Publikováno v:
Journal of Nepal Paediatric Society. 35:312-313
Caffey's disease is a rare, self limiting condition of infancy. Most commonly mandible, clavicle and ulna are affected leading to inflammation of periosteum and overlying soft tissue. We here present an 1 year 3 month old girl with features of Caffey
Publikováno v:
Journal de Radiologie. 89:1767-1769
Publikováno v:
International Journal of Biomedical and Advance Research. 7:482
Infantile cortical hyperostosis (Caffey disease) is characterized by spontaneous episodes of subperiosteal new bone formation along 1 or more bones commencing within the first 5 months of life.It is featured by acute inflammation of periosteum and ov
Publikováno v:
Collegium antropologicum
Volume 31
Issue 1
Volume 31
Issue 1
The case of a six-month old boy with mandibular Caffey’s disease is described. Emphasis is placed on the role of bone scintigraphy, as a diagnostic method which would be, because of the clinical picture and the beginning of the disease (suspected o
Autor:
Hajnžić, Tomislav Franjo, Markičević, Karmen, Vrsalović, Renata, Hat, Josip, Kovačić, K, Kokoš, Željka, Mataija, Marina
Caffey disease, also called infantile cortical hyperostosis, is a bone disorder that most often occurs in babies. Excessive new bone formation (hyperostosis) is characteristic of Caffey disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::f533c7b2c0b38f143049e46d5ae1a274
https://www.bib.irb.hr/1177586
https://www.bib.irb.hr/1177586