Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Candice Jacinta Antao"'
Publikováno v:
Journal of Oral Research and Review, Vol 10, Iss 2, Pp 87-91 (2018)
Crouzon's syndrome is a rare genetic disorder characterized by distinctive craniofacial malformations. The disease is characterized by premature synostosis of coronal and sagittal sutures which begins in the 1st year of life. Herein, we report a case
Externí odkaz:
https://doaj.org/article/688da44c7e8e4c5e8188c37e6104973d
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 12, Pp ZD14-ZD17 (2018)
Dystrophic calcinosis is a condition wherein calcium is deposited in degenerated tissues, often associated with trauma, infection, or inflammation, in the absence of a systemic mineral imbalance. It commonly occurs in cardiac and skeletal muscles; r
Externí odkaz:
https://doaj.org/article/d1d2d66a6382458da7d91581a0c74b19
Publikováno v:
Annals of Maxillofacial Surgery
Chronic diffuse sclerosing osteomyelitis (CDSO) is a disease that presents a rather unusual clinicoradiographic picture creating diagnostic and therapeutic problems. Involvement of the temporomandibular joint is not frequently observed in CDSO. We re
Publikováno v:
Indian Journal of Case Reports. 4:515-518
Glandular odontogenic cyst (GOC) is a rare developmental odontogenic cyst that has gained special attention primarily due to its aggressive potential and the microscopic features, it shares with central mucoepidermoid carcinoma of the jaws. This rela
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 12, Pp ZD14-ZD17 (2018)
Dystrophic calcinosis is a condition wherein calcium is deposited in degenerated tissues, often associated with trauma, infection, or inflammation, in the absence of a systemic mineral imbalance. It commonly occurs in cardiac and skeletal muscles; ra
Publikováno v:
Journal of Oral Research and Review, Vol 10, Iss 2, Pp 87-91 (2018)
Crouzon's syndrome is a rare genetic disorder characterized by distinctive craniofacial malformations. The disease is characterized by premature synostosis of coronal and sagittal sutures which begins in the 1st year of life. Herein, we report a case
Publikováno v:
Journal of Oral Medicine, Oral Surgery, Oral Pathology and Oral Radiology. 2:94