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of 68
pro vyhledávání: '"Segmental odontomaxillary dysplasia"'
Akademický článek
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Publikováno v:
Journal of Indian Society of Pedodontics and Preventive Dentistry, Vol 32, Iss 1, Pp 83-86 (2014)
Segmental odontomaxillary dysplasia is a type of hemi-maxillofacial dysplasia. It is a sporadic, mesoectodermal dysplasia that presents early in life, possibly as early as in utero and exhibits male gender predominance (1.7:1.0). Its features include
Externí odkaz:
https://doaj.org/article/48b66e69ef4c4693bd1eaebdecf62197
Publikováno v:
Indian Journal of Dental Research, Vol 25, Iss 1, Pp 102-106 (2014)
Segmental odontomaxillary dysplasia (SOD) is an uncommon, nonhereditary, rare developmental disorder primarily involving the posterior part of the maxilla and related dental components. It is a rare condition of uncertain etiology that results in pai
Externí odkaz:
https://doaj.org/article/4010f8618ba84dfdb8c936e9b7718a47
Autor:
Daniele Torchia
Publikováno v:
Journal of the American Academy of Dermatology. 85:e101-e103
Publikováno v:
International Journal of Oral and Dental Health. 6
Akademický článek
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Autor:
Shola Todd
Publikováno v:
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. 132:e48-e49
Introduction Segmental odontomaxillary dysplasia (SOD) is a rare nonhereditary developmental disorder of the maxilla. It is characterized by painless unilateral enlargement of the right or left maxillary alveolar bone. In the enlarged region, dental
Publikováno v:
Head Neck Pathol
Segmental odontomaxillary dysplasia (SOD) is a developmental condition of the middle and posterior maxilla featuring dysplastic bone overgrowth, dental abnormalities and, occasionally, various homolateral cutaneous manifestations. Herein, we describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::920bb6056dc5b1616c58495d0e4b1b27
https://europepmc.org/articles/PMC8010023/
https://europepmc.org/articles/PMC8010023/
Autor:
Abdullah Alakeel
Publikováno v:
Cureus
Hemimaxillary enlargement, asymmetry of the face, tooth abnormalities, and skin findings (HATS) syndrome, a rare developmental disorder, involves the first and second branchial arches and is characterized by hemimaxillary enlargement, abnormal appear
Autor:
Anna C. Thomas, L. Solman, Satyamaanasa Polubothu, Neil W. Bulstrode, Lisa Weibel, J. Obwegeser, Dalia Abdin, Raoul C.M. Hennekam, M. Barysch, Veronica A. Kinsler, Alistair Calder, N. Di Donato, R. Evans
Publikováno v:
British journal of dermatology, 183(6), 1128-1130. Wiley-Blackwell
Segmental odontomaxillary dysplasia (SOD) is a rare condition of unknown incidence, with approximately 60 cases reported (as reviewed in 2018)1 . It presents at birth or during childhood with a constellation of ipsilateral facial signs: non-progressi