amelogenesis वाक्य
उदाहरण वाक्य
मोबाइल
- The AMELX gene encodes for the structural modeling protein, amelogenin, which works with other amelogenesis-related proteins to direct the mineralisation of enamel.
- Mutations in the AMELX gene can result in amelogenesis imperfecta, which refers to the collection of enamel defects resulting from either genetic or environmental causes.
- The presence of this hair texture type is a defining characteristic between a diagnosis of "'TDO "'verses amelogenesis imperfecta with hypomaturation.
- Enamel mineralization only occurs once ( as ameloblasts are lost with eruption within the reduced enamel epithelium ); therefore after amelogenesis, enamel production has been finalized.
- People afflicted with amelogenesis imperfecta have teeth with abnormal color : yellow, brown or grey; this disorder can afflict any number of teeth of both dentitions.
- There are some physical symptoms that have been associated with KTS . The most prominent symptom is amelogenesis imperfecta which gives the teeth a stained brown-yellow color.
- Amelogenesis imperfecta, an abnormal formation of the enamel or external layer of the crown of the tooth, may also be present where the tooth enamel may be thin or absent.
- Enamel spindles are also linear defects, but they too can be found only at the DEJ, because they are formed by entrapment of odontoblast processes between ameloblasts prior to and during amelogenesis.
- Furthermore, individuals with the disorders of orofacial complex such as Amelogenesis imperfecta, Dentinogenesis imperfecta, Cleft lip / palate, oral cancer and a like, are also considered as special health care need patients.
- There are several clinical subsets of amelogenesis imperfecta, but common to TDO is the hypoplastic-hypomaturation subtype; the hypomaturation-hyoplastic is less common in individuals with "'TDO " '.
- The hypoplastic-hypomaturation type of amelogenesis imperfecta with "'TDO "'occurs where the tooth enamel depicts a generalized pitted pattern, with open contacts between the teeth as well as an open bite.
- Amelogenesis imperfecta, which occurs in between 1 in 718 and 1 in 14, 000 individuals, is a disease in which the enamel does not fully form or forms in insufficient amounts and can fall off a tooth.
- In most cases, males with an X-linked form of this condition experience more severe dental abnormalities than affected females . Recent genetic studies suggest that the cause of a significant proportion of amelogenesis imperfecta cases remains to be discovered.
- "' Kohlsch�tter-T�nz syndrome "'( KTS ), also called "'Amelo-cerebro-hypohidrotic syndrome "'is a rare inherited syndrome characterized by epilepsy, dementia, intellectual disability, and yellow teeth caused by amelogenesis imperfecta ( abnormal formation of tooth enamel ).
- It is phenotypically difficult to diagnose between "'TDO "'and Amelogenesis imperfecta of the hypomaturation-hypoplasia type with taurodontism ( AIHHT ) as they are very closely linked phenotypically during adulthood, and the only distinguishing characteristic is found during genetic analysis by Polymerase Chain Reaction ( PCR ) amplification.
- :: : : : I think that this is probably congenital, since I've had it for as long as I remember, unless that bout of meningitis did more than just give me a mild case of " amelogenesis imperfecta " . talk ) 23 : 54, 11 September 2014 ( UTC)
- Amelogenesis imperfecta of the hypomaturation type with taurodontism ( AIHHT ) has no hair or bone changes which helps to differentiate between " TDO " cases and AIHHT . Polymerase Chain Reaction also known as PCR is used to amply pieces of DNA and observed for the 141 base pair allele as a result of a deletion of four nucleotides in exon 3 of the DLX-3 gene.
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