Higher frequency of uncommon 1.5–2 Mb deletions found in familial cases of 22q11.2 deletion syndrome

✍ Scribed by Luis Fernández; Pablo Lapunzina; Isidora López Pajares; Germán Rodríguez Criado; Luis García-Guereta; Jesús Pérez; José Quero; Alicia Delicado

• Publisher: John Wiley and Sons
• Year: 2005
• Tongue: English
• Weight: 105 KB
• Volume: 136A
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.30756

✦ Synopsis

Abstract

Familial 22q11.2 deletions have been reported as a 6%–28% of the total affected cases of 22q11.2 microdeletion syndrome (del22q11.2). Different deletion genotypes have been described for this disorder, with a predominant 3 Mb deletion present in 90% of the cases, a less common 1.5–2 Mb deletion in 8%, and atypical smaller deletions in 2%. We have studied 15 cases of del22q11.2 from 6 families (two of them three‐generation families) that were previously diagnosed through FISH. We have sized the deleted region by allele genotyping of 12–16 polymorphic markers in all cases, and we have found three families affected with the 1.5–2 Mb deletion, two affected with the 3 Mb deletion, and one in which the deletion size could not be determined. This predominance of the smaller 1.5–2 Mb deletions in our familial cases differs from the minor frequency observed in sporadic cases of del22q11.2. This finding suggests that small deletions are more linked to familial inheritance than large ones, possibly due to psychosocial or biological factors associated with differences in the phenotype. Deletion sizing on routine diagnosis may help characterizing the inheritability of 22q11.2 microdeletion syndrome. © 2005 Wiley‐Liss, Inc.