Familiar del3p syndrome: The uncertainty of the prognosis. A case report

Abstract

Abstract The 3p deletion syndrome is an unusual condition. The few cases described are mainly de novo. We described a familial case detected in a prenatal diagnosis. Three members of the family had the 3p26.3‐p26.1 deletion; however, only the son presented clinical features.

Keywords

• 3p deletion
• array‐comparative genomic hybridization
• cytogenetic
• fluorescence in situ hybridization