| Literature DB >> 28488400 |
Carolyn C Jackson1,2,3, Alain Lefèvre-Utile4, Anne Guimier5, Valérie Malan5, Julie Bruneau6, Antoine Gessain7, Olivier Cassar7, Jeanne Amiel5, Aurélie Cobat8,9, Vimel Rattina8,9, Laurent Abel1,8,9, Jean-Laurent Casanova1,4,8,9,10, Stéphane Blanche4.
Abstract
Chromosome 7 germline macrodeletions have been implicated in human congenital malformations and developmental delays. We herein report a novel heterozygous macrodeletion of 7q34-q36.3 in a 16-year-old girl originally from West Indies. Similar to previously reported cases of germline chromosome 7q terminal deletions, our patient has dental malposition, and developmental (growth and intellectual) delay. Novel phenotypic features include endemic Kaposi sarcoma (KS), furrowed tongue, thoracolumbar scoliosis, and mild mitral valve dysplasia. The occurrence of human herpes virus 8-driven KS, in a child otherwise normally resistant to other infectious agents and without any other tumoral lesion, points to a very selective immunodeficiency. While defects in organogenesis have been described with such macrodeletions, this is the first report of immunodeficiency and cancer predisposition.Entities:
Keywords: Kaposi sarcoma; chromosome 7 deletion; human herpes virus-8
Year: 2017 PMID: 28488400 PMCID: PMC5680148 DOI: 10.1002/ajmg.a.38275
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802