Search for a gene responsible for Floating-Harbor syndrome on chromosome 12q15q21.1.

Abstract

Floating-Harbor syndrome (FHS) is characterized by characteristic facial dysmorphism, short stature with delayed bone age, and expressive language delay. To date, the gene(s) responsible for FHS is (are) unknown and the diagnosis is only made on the basis of the clinical phenotype. The majority of cases appeared to be sporadic but rare cases following autosomal dominant inheritance have been reported. We identified a 4.7 Mb de novo 12q15-q21.1 microdeletion in a patient with FHS and intellectual deficiency. Pangenomic 244K array-CGH performed in a series of 12 patients with FHS failed to identify overlapping deletions. We hypothesized that FHS is caused by haploinsufficiency of one of the 19 genes or predictions located in the deletion found in our index patient. Since none of them appeared to be good candidate gene by their function, a high-throughput sequencing approach of the region of interest was used in eight FHS patients. No pathogenic mutation was found in these patients. This approach failed to identify the gene responsible for FHS, and this can be explained by at least four reasons: (i) our index patient could be a phenocopy of FHS; (ii) the disease may be clinically heterogeneous (since the diagnosis relies exclusively on clinical features), (iii) these could be genetic heterogeneity of the disease, (iv) the patient could carry a mutation in a gene located elsewhere. Recent descriptions of patients with 12q15-q21.1 microdeletions argue in favor of the phenocopy hypothesis.

• Authors: Estelle Lopez, Patrick Callier, Valérie Cormier-Daire, Didier Lacombe, Anne Moncla, Armand Bottani, Sandy Lambert, Alice Goldenberg, Bérénice Doray, Sylvie Odent, Damien Sanlaville, Lucie Gueneau, Laurence Duplomb, Frédéric Huet, Bernard Aral, Christel Thauvin-Robinet, Laurence Faivre
• Journal: American journal of medical genetics. Part A (Am J Med Genet A) Vol. 158A Issue 2 Pg. 333-9 (Feb 2012) ISSN: 1552-4833 [Electronic] United States
• PMID: 22247066 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2012 Wiley Periodicals, Inc.

Topics

• Abnormalities, Multiple (genetics, pathology)
• Adult
• Child
• Child, Preschool
• Chromosomes, Human, Pair 12 (genetics)
• Comparative Genomic Hybridization (methods)
• Craniofacial Abnormalities (genetics, pathology)
• Female
• Genetic Predisposition to Disease
• Growth Disorders (genetics, pathology)
• Haploinsufficiency (genetics)
• Heart Septal Defects, Ventricular (genetics, pathology)
• High-Throughput Nucleotide Sequencing
• Humans
• Male
• Phenotype
• Sequence Deletion (genetics)