Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Amit R. Parate"'
Publikováno v:
Journal of Oral Biology and Craniofacial Research, Vol 11, Iss 4, Pp 529-535 (2021)
Pycnodysostosis is a rare autosomal recessive condition caused by the mutation of CTSK gene. CTSK regulates the activity of Cathepsin K which is responsible for osteoclast-mediated bone resorption. This mutation causes the bones to become dense, scle
Externí odkaz:
https://doaj.org/article/ee3d4d78ff4e4ffe9ddcb61d6f87be6c
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-3 (2020)
Abstract Background Parafunctional oral habits are known to cause deleterious effects on maxillofacial structures. One such effect is traumatic injuries secondary to chewing inanimate objects like pencils. Following trauma, the lead of the pencil has
Externí odkaz:
https://doaj.org/article/0132174b62b54364980e71ac913fc8bc
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 33, Iss 1, Pp 95-98 (2021)
Mc Cune Albright Syndrome (MAS) is a rare, sporadic disorder characterized by a triad of symptoms: fibrous dysplasia, cafe-au-lait spots, and endocrinopathy. It is thought to be caused by the mutation of the GNAS1 gene and is predominantly a disease
Externí odkaz:
https://doaj.org/article/c7a7f555bbd842c6aa0568bd2f084671
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 32, Iss 4, Pp 417-420 (2020)
Herpes Zoster (HZ) is an acute vesiculobullous condition affecting dermatomes supplied by cranial or extracranial nerves. It is caused by reactivation of varicella zoster virus (VZV) in a patient with a history of chickenpox. Usually, a single dermat
Externí odkaz:
https://doaj.org/article/9489d33a60bf4fe6b979c09f2b765956
Publikováno v:
J Oral Biol Craniofac Res
Pycnodysostosis is a rare autosomal recessive condition caused by the mutation of CTSK gene. CTSK regulates the activity of Cathepsin K which is responsible for osteoclast-mediated bone resorption. This mutation causes the bones to become dense, scle
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 33, Iss 1, Pp 95-98 (2021)
Mc Cune Albright Syndrome (MAS) is a rare, sporadic disorder characterized by a triad of symptoms: fibrous dysplasia, cafe-au-lait spots, and endocrinopathy. It is thought to be caused by the mutation of the GNAS1 gene and is predominantly a disease
Autor:
Amit R. Parate, Dinesh Naitam, Suryakant C Deogade, Arun N. Khalikar, Sushant M. Patil, Snehal Bansod
Publikováno v:
Open Journal of Stomatology. 11:422-436
Publikováno v:
BMC Pediatrics
BMC Pediatrics, Vol 20, Iss 1, Pp 1-3 (2020)
BMC Pediatrics, Vol 20, Iss 1, Pp 1-3 (2020)
Background Parafunctional oral habits are known to cause deleterious effects on maxillofacial structures. One such effect is traumatic injuries secondary to chewing inanimate objects like pencils. Following trauma, the lead of the pencil has been rep
Publikováno v:
International Journal of Medical and Dental Case Reports. 4:1-4
Publikováno v:
Journal of Oral Research and Review. 13:139
Congenital midline labial sinus is a rare condition known to affect both the upper and the lower lip. This anomaly has been reported in both genders, but with a slightly increased predilection in females. It can occur either in isolation or in associ