Most of the time, 22q11.2 Deletion syndrome results from a new genetic deletion that occurs when a baby is conceived. It is located at a specific place on that chromosome called q11.2. The name of the syndrome denotes the missing piece of chromosome 22. To Know more facts about 22q11.2 Deletion Syndrome Market Report, Click Here : As per several studies, it is the most common chromosomal microdeletion reported in humans. In the 7MM, of the focused age-group 6 to 12 and 13 to 17 years, the diagnosed prevalent cases of 22q11.2 deletion syndrome with Behavioral and Psychiatric Phenotypes were 36,702, in 2020.Ģ2q11.2 Deletion Syndrome is a condition that develops because of chromosome defects and is a complex, multi-organ disorder noted for its varying severity and penetrance among those affected.

Ē2q11.2 deletion syndrome is a multisystem disorder characterized by several physical, behavioral and psychiatric disorders.In the EU-5 countries, the total diagnosed prevalent cases of 22q11.2 deletion syndrome were 35,203 in 2020. Ē2q11.2 deletion syndrome is often underdiagnosed and misdiagnosed, as the symptoms vary from patient to patient.

Ěmong the EU-5 countries, the highest number of cases of 22q11.2 deletion syndrome were in Germany and the least in Spain in 2020.The United States, in the same year, accounted for 83,326 cases, the highest prevalence of 22q11.2 deletion syndrome cases in the 7MM, accounting for approximately 42% of the total 7MM cases in 2020. In 2020, the total prevalent cases of 22q11.2 deletion syndrome were 196,476 in the 7MM.

Some facts of 22q11.2 Deletion Syndrome Market are:

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