Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Vinod Vijay Chandar"'
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 28, Iss 2, Pp 207-210 (2016)
Noonan syndrome is a clinically and genetically heterogeneous condition characterized by distinctive facial features, short stature, chest deformity, congenital heart diseases and other comorbidities. It is an autosomal dominant disorder with complet
Externí odkaz:
https://doaj.org/article/faed4ad509eb48a081907cb0b05dc2c1
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 27, Iss 3, Pp 437-440 (2015)
Oligodontia, a rare genetic disorder, represents the congenital absence of more than six teeth in primary, permanent, or both dentitions and is usually the feature of a syndrome. Its occurrence as an isolated entity is even rarer. This article report
Externí odkaz:
https://doaj.org/article/2277aa6dcf464e9187e9e60de8edd8ec
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 27, Iss 2, Pp 286-290 (2015)
A painless, bluish, submucosal swelling on one side of the floor of the mouth usually indicates the presence of a ranula. Rarely, such a swelling may be caused by an inflammatory disease process in a salivary gland, a neoplasm in the sublingual saliv
Externí odkaz:
https://doaj.org/article/657c1270a5e94d24a3127e40266c3d7c
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 27, Iss 1, Pp 115-118 (2015)
Among the eruption disorders, the most common developmental dental anomalies encountered are the retention or impaction of teeth. Impaction of multiple teeth is a common finding associated with some syndromes or systemic disorders. This is a report o
Externí odkaz:
https://doaj.org/article/bb560d590172406e991e73c5b62f417e
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 26, Iss 4, Pp 467-472 (2014)
The new millennium has witnessed a sea change in diagnostic imaging sciences and the unfortunate ′tilt′ toward ′over imaging′ and ′over relying′ on modern imaging needs to be relooked. This case report emphasizes the need to strengthen co
Externí odkaz:
https://doaj.org/article/badcc6df6610445883703ec2091d0245
Autor:
Vinod Vijay Chandar, M Venkateswarlu
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 21, Iss 1, Pp 12-16 (2009)
Objectives : This study was aimed at evaluating the utility of ultrasonography in the diagnosis and treatment plan of certain orofacial lesions over the clinical and radiological evaluation of patients and to visualize advantages and disadvantages, i
Externí odkaz:
https://doaj.org/article/27145f509f1e4c0a8557da8985764c62
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 28, Iss 2, Pp 207-210 (2016)
Noonan syndrome is a clinically and genetically heterogeneous condition characterized by distinctive facial features, short stature, chest deformity, congenital heart diseases and other comorbidities. It is an autosomal dominant disorder with complet
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 27, Iss 3, Pp 437-440 (2015)
Oligodontia, a rare genetic disorder, represents the congenital absence of more than six teeth in primary, permanent, or both dentitions and is usually the feature of a syndrome. Its occurrence as an isolated entity is even rarer. This article report
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 27, Iss 2, Pp 286-290 (2015)
A painless, bluish, submucosal swelling on one side of the floor of the mouth usually indicates the presence of a ranula. Rarely, such a swelling may be caused by an inflammatory disease process in a salivary gland, a neoplasm in the sublingual saliv
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 26, Iss 4, Pp 467-472 (2014)
The new millennium has witnessed a sea change in diagnostic imaging sciences and the unfortunate ′tilt′ toward ′over imaging′ and ′over relying′ on modern imaging needs to be relooked. This case report emphasizes the need to strengthen co