We report a child with a unique combination of 22q11 deletion syndrome and 14q terminal deletion syndrome. deafness and renal malformations are typical [Schuffenhauer et al., 1995]. Although most 22q11.2 deletions occur sporadically, it is estimated that 8C28 % of deletions are inherited from a parental carrier [Driscoll et al., 1993; Hall, 1993; Ryan et… Continue reading We report a child with a unique combination of 22q11 deletion