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Corneal dystrophies are bilateral, usually well-proportioned groups of periodic inherited ailments of the cornea. Modifications in some distinct genes on various centromeres are related to Corneal dystrophy. This examination is valuable for the hereditary conclusion of this ailment.
A duly reloaded Whole Exome Sequencing Agreement Form is compulsory.
Corneal Dystrophies are a gathering of congenital, typically refined, eye ailments in which abnormal material often amasses in the obvious outer layer of the cornea.
The beginning of manifestation differs between patients, from asymptomatic to substantial imagination impairment topics. This ailment can either influence one or both corneas and the passion of manifestation , in that circumstance, are not necessarily identical. The age of beginning and precise symptoms differ among the distinct forms of corneal dystrophy. CD can be placed by which coatings of the cornea are dramatic:
The Igenomix sclera Dystrophies Precision Panel can be utilized to make a corrected and supervised diagnosis directing to better management and prediction of the ailment. It delivers a comprehensive calculation of the genes implicated in this ailment using next-generation sequencing to completely apprehend the expanse of relevant genes implicated.
The Igenomix Corneal Dystrophies Precision Panel is demonstrated for those patients with a clinical infection or apprehension presenting with or without the followership embodiments:
The clinical usefulness of this conference is:
The hereditary and molecular assurance for correct clinical detection of a symptomatic patient.
Premature initiation of multidisciplinary antidote comprising a traditional follow-up in case of asymptomatic patients. Sight drops and ointments can be utilized in the possibility of mild manifestation. Surgical antidotes can be evaluated if the failure of imagination is brutal sufficiently.
Risk assessment and hereditary counseling of asymptomatic family constituents according to the method of heritage.
Modification of illustration of genotype-phenotype correlation.
| Test Type | Nx Gen Sequencing: Corneal Dystrophy |
| Includes | Nx Gen Sequencing: Corneal Dystrophy Test (Ophthalmology) |
| Preparation | |
| Reporting | Within 24 hours* |
| Test Price |
₹ 15925
|
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