Your doctor will need to have an examination and tests if you have an infertility problem to determine the cause and choose the appropriate treatment. Checking your test results can help your doctor choose the best treatment for your infertility.

The first three months of screening tests usually take between 1 and 2 weeks. The first trimester of screening allows the mother to be aware of any potential problems as soon as possible. Screening tests only determine the risk of the fetus having a chromosomal or genetic disorder and by no means does it imply a definitive disorder.

In real-time PCR, the most accurate and reliable results are obtained using a fluorescence probe. A wide range of hereditary diseases can also be found, including hereditary diseases (API-1, Factor V Liden, Factor II MTHFR), hereditary infertility diseases, (Androgen insenstivity, Congenital adrenal hyperplasia, Pseudohermaphroditism, etc.). Neuromuscular, hereditary patients examined immune deficiency, metabolic diseases, and cancers.

These tests are also important for: Treatment of the disease / Monitoring the progress of the disease / Preventing the disease (eg, Pap smears or mammograms may reduce the risk of some common cancers in women through early detection) / Determination Risk of disease (eg, cholesterol levels observed or risk of inherited diseases such as familial breast cancer)

Immunology and serology tests, diagnostic tests such as bacterial, viral, mycoplasma, parasitic, complement deficiency, monoclonal, polyclonal and immunoglobulin deficiency tests, as well as tests for autoimmune diseases such as multiple sclerosis, Lupus, rheumatoid arthritis is performed by methods such as immunofluorescence.

Major tests performed in microbiology include: urine, throat, antibiotic samples such as sputum, Chlamydia-Mycoplasma antigen testing, fungal excretion, rotavirus stool antigen testing, diagnostic tests for hepatitis and other diseases, testing Antigen and microscopy of parasitic diseases such as Amoeba and Giardia

The simplest and most important test in this section is blood cell count and morphology study of blood cells to detect different types of anemia, malignancies, and so on. In this section hemophilia and thalassemia can be diagnosed. The most important of these can be platelet count, examination of their shape and size, which can be helpful in the diagnosis of hemophilia or platelet disorders.

Routine biochemical tests performed in the biochemical laboratory include tests such as BUN, creatinine, creatinine clearance, AST, ALT, and others. Electrolytes named calcium, phosphorus, iron, iron binding capacity, ferritin, vitamin B12, folic acid, blood gases, heart tests, CK-MB mass, troponin T and troponin I, dimer. Complete urine testing, a 2-hour urine test, and protein testing are also performed