Molecular diagnosis

From WikiMD's Wellness Encyclopedia

Molecular diagnosis is a technique used in medical diagnosis to identify a disease or condition by analyzing molecules, such as proteins or nucleic acids, in a patient's tissue or fluid. This technique is often used in the diagnosis of genetic disorders, infectious diseases, and certain types of cancer.

Overview[edit | edit source]

Molecular diagnosis involves the analysis of DNA or RNA sequences, including the identification of mutations or variations that may be associated with disease. This can involve techniques such as polymerase chain reaction (PCR), DNA sequencing, and microarray analysis.

Techniques[edit | edit source]

Polymerase Chain Reaction[edit | edit source]

Polymerase chain reaction (PCR) is a common technique used in molecular diagnosis. It involves the amplification of a specific DNA sequence, allowing for the detection of even small amounts of a specific DNA or RNA sequence. This can be useful in the diagnosis of infectious diseases, as it can detect the presence of a specific pathogen's DNA or RNA in a patient's sample.

DNA Sequencing[edit | edit source]

DNA sequencing is another technique used in molecular diagnosis. It involves determining the precise order of nucleotides within a DNA molecule. This can be useful in the diagnosis of genetic disorders, as it can identify mutations or variations in a patient's DNA that may be associated with a specific disease or condition.

Microarray Analysis[edit | edit source]

Microarray analysis is a technique used in molecular diagnosis that involves the simultaneous detection of many different DNA or RNA sequences in a sample. This can be useful in the diagnosis of certain types of cancer, as it can identify changes in gene expression that may be associated with the disease.

Applications[edit | edit source]

Molecular diagnosis has a wide range of applications in medicine. It is often used in the diagnosis of genetic disorders, infectious diseases, and certain types of cancer. It can also be used in prenatal diagnosis to identify genetic disorders in a fetus, and in pharmacogenomics to determine a patient's likely response to certain medications.

See Also[edit | edit source]

Molecular diagnosis Resources
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Contributors: Prab R. Tumpati, MD