Velocardiofacial Syndrome

It is possible that the main title of the record Chromosome 22q11.2 Removal Syndrome is not the name you anticipated. Kindly check the basic synonyms specifying to locate the alternating name(s) and also problem class(s) covered by this rating.


  • DiGeorge disorder
  • velocardiofacial disorder
  • Shprintzen disorder
  • conotruncal anomaly face syndrome
  • Caylor cardiofacial syndrome
  • autosomal leading Opitz G/BBB syndrome

Condition Communities

  • None

General Conversation
Chromosome 22q11.2 removal disorder is related to an array of problems consisting of: hereditary heart illness, taste buds abnormalities, immune system disorder consisting of autoimmune illness, low calcium (hypocalcemia) and also other endocrine problems such as thyroid problems and development hormone shortage, intestinal problems, feeding difficulties, kidney irregularities, hearing loss, seizures, skeletal irregularities, small facial differences, as well as knowing and behavioral distinctions. The signs and symptoms of this problem are exceptionally variable, even amongst members of the exact same family members.

Chromosome 22q11.2 removal disorder is a condition dued to a little item of chromosome 22 missing. A variety of independently described medical diagnoses including DiGeorge syndrome (DGS), velocardiofacial syndrome (VCFS), conotruncal irregularity face disorder (CTAF), autosomal dominant OpitzG/BBB disorder as well as Cayler Cardiofacial disorder were all initially believed to be separate problems before the chromosome 22q11. 2 deletion was determined in people influenced with every one of these problems.

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