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Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes
Author(s) -
Gervasini C,
Pfundt R,
Castronovo P,
Russo S,
Roversi G,
Masciadri M,
Milani D,
Zampino G,
Selicorni A,
Schoenmakers EFPM,
Larizza L
Publication year - 2008
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2008.01086.x
Subject(s) - cornelia de lange syndrome , gene duplication , comparative genomic hybridization , genetics , biology , phenotype , copy number variation , gene , mutation , genetic heterogeneity , genome
Cornelia de Lange syndrome (CdLS) is a rare, multiple congenital anomaly/mental retardation syndrome characterized by varied clinical signs including facial dysmorphism, pre‐ and post‐natal growth defects, small hands and malformations of the upper limbs. Established genetic causes include mutations in the NIPBL (50–60%), SMC1L1 and SMC3 (5%) genes. To detect chromosomal rearrangements pointing to novel positional candidate CdLS genes, we used array‐CGH to analyze a subgroup of 24 CdLS patients negative for mutations in the NIPBL and SMC1L1 genes. We identified three carriers of DNA copy number alterations, including a de novo 15q26.2‐qter 8‐Mb deletion, and two inherited 13q14.2‐q14.3 1‐Mb deletion and 13q21.32‐q21.33 1.5‐Mb duplication, not reported among copy number variants. The clinical presentation of all three patients matched the diagnostic criteria for CdLS, and the phenotype of the patient with the 15qter deletion is compared to that of both CdLS and 15qter microdeletion patients.