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It is a cytogenetic test that is used in diagnosis of oligodendrogliomas.
Oligodendrogliomas is a rare type of tumour of central nervous system (brain and spinal cord). Oligodendrogliomas are a subtype of gliomas, or primary brain tumours. They occur more often in men around the age group of 35-45years. It can be of low or high grade. The common symptoms of this tumour are:
Oligodendrogliomas usually have deletion of short arm of chromosome 1(1p)and long arm of chromosome 19(19q).Thus 1p19q codeletion test is a useful adjunct in the diagnosis of this rare tumour and to differentiate it from other types of glioma. Oligodendrogliomas are mainly treated by surgery, chemotherapy and radiotherapy.
Fluorescent in situ hybridisation (FISH)-it is an advanced and accurate test that maps the genetic material (DNA) present on the chromosomes in cells. It helps to look at specific gene or portion of gene to detect abnormalities.
It includes detection of1p36 deletion and 19q13 deletion with help of FISH probes.
1p 19 q codeletion FISH test is done on tumour biopsy tissue which is taken out by inserting a needle into the tumour through a small hole in skull. Relevant clinical history/physical examination findings must be sent along with the sample. A properly filled requisition form must accompany the sample.