22q11.2 deletion syndrome

22q11.2 deletion syndrome (DS) is a chromosomal anomaly which causes a congenital malformation disorder whose common features include cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency.

Anemia

A reduction in erythrocytes volume or hemoglobin concentration.


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PMID (PMCID)
2788242
 MALE Infant
[Graft versus host reaction in an infant with DiGeorge syndrome].
Wintergerst U, Meyer U, Remberger K, Belohradsky BH.
Monatsschr Kinderheilkd. 1989;137(6):345-7.
An infant with complete DiGeorge syndrome was treated with blood transfusions and fresh frozen plasma because of severe septicemia and anemia.