It is feasible that the primary title of the rating Chromosome 22q11.2 Removal Syndrome is not the name you expected. Please examine the words listing to find the alternating name(s) and problem community(s) covered by this report.
- DiGeorge disorder
- velocardiofacial syndrome
- Shprintzen syndrome
- conotruncal abnormality face disorder
- Caylor cardiofacial syndrome
- autosomal leading Opitz G/BBB syndrome
Chromosome 22q11.2 deletion disorder is connected with an array of issues consisting of: genetic heart illness, palate abnormalities, body immune system disorder including autoimmune condition, low calcium (hypocalcemia) as well as various other endocrine irregularities such as thyroid troubles and also growth bodily hormone deficiency, intestinal troubles, feeding problems, kidney irregularities, hearing loss, seizures, skeletal abnormalities, small face differences, and also discovering and also behavior differences. The signs and symptoms of this condition are very variable, also amongst members of the very same family members.
Chromosome 22q11.2 removal syndrome is a disorder dued to a little item of chromosome 22 missing out on. A variety of independently explained diagnoses consisting of DiGeorge syndrome (DGS), velocardiofacial disorder (VCFS), conotruncal irregularity face disorder (CTAF), autosomal leading OpitzG/BBB syndrome as well as Cayler Cardiofacial syndrome were all initially thought to be separate conditions prior to the chromosome 22q11. 2 deletion was determined in individuals affected with all of these problems.