What does 22q11.2 deletion syndrome mean?

Definitions for 22q11.2 deletion syndrome

Here are all the possible meanings and translations of the word 22q11.2 deletion syndrome.

Freebase

  1. 22q11.2 deletion syndrome

    22q11.2 deletion syndrome, which has several presentations including DiGeorge syndrome, DiGeorge anomaly, velo-cardio-facial syndrome, Shprintzen syndrome, conotruncal anomaly face syndrome, Strong syndrome, congenital thymic aplasia, and thymic hypoplasia, is a syndrome caused by the deletion of a small piece of chromosome 22. The deletion occurs near the middle of the chromosome at a location designated 22q11.2—signifying its location on the long arm of one of the pair of chromosomes 22, on region 1, band 1, sub-band 2. It has a prevalence estimated at 1:4000. The syndrome was described in 1968 by the pediatric endocrinologist Angelo DiGeorge. 22q11 deletion is also associated with truncus arteriosus.

Numerology

  1. Chaldean Numerology

    The numerical value of 22q11.2 deletion syndrome in Chaldean Numerology is: 3

  2. Pythagorean Numerology

    The numerical value of 22q11.2 deletion syndrome in Pythagorean Numerology is: 7

Images & Illustrations of 22q11.2 deletion syndrome

  1. 22q11.2 deletion syndrome22q11.2 deletion syndrome22q11.2 deletion syndrome

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