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Y Chromosome Microdeletions

Includes 1 test
Blood
130€

Molecular control for micro-chromosome Y defects is used in the evaluation of men with azoospermia, severe oligozoospermia or other unexplained infertility.

More information

Υ chromosome microdeletion (YCM) is a family of genetic disorders caused by the lack of a gene or genes on the Υ chromosome. Many men with Υ chromosome microdeletion have no symptoms and live a normal life. However, micro-defects of the Υ chromosome are known to be present in a significant number of men with reduced fertility. The microarrays refer to three regions located on the long arm of the Υ chromosome: AZFa, AZFb and AZFc.

Infertility due to microleakage of the Υ chromosome is characterized by azoospermia (absence of semen), severe oligozoospermia (<1 x  106 spermatozoa / mL), moderate oligozoospermia (1-5 x  106 spermatozoa / mL) or mild oligozoospermia (5-15 x  106 spermatozoa / mL) . Men with infertility due to Y chromosome microdeletion usually have no obvious symptoms, although a physical examination may reveal small testes.

Suspected infertility due to micro deficiencies of the Υ chromosome can be raised in otherwise healthy men with azoospermia or oligozoospermia or abnormal morphology of the spermatozoa and also impaired motility of the spermatozoa and other spermatozoa.

In cases of micro-Υ chromosome abnormalities, pregnancy can be achieved by in vitro fertilization using ICSI (intracytoplasmic sperm injection), a fertilization process in which sperm can be recovered by ejaculation (ejaculation) in men with azoospermia). Recovery of sperm from testicular biopsy for IVF is not effective for men with AZFb and AZFa deficiencies but is successful for most men with AZFc deficiencies. The risk of genetic abnormalities is the same as in any infertile couple using assisted reproduction techniques.

The Υ chromosome-derived infertility is inherited in a Υ-linked manner. As males with Y chromosome defects are sterile, deficiencies usually appear de novo.

 

 

 

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