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Kaposi sarcoma, oral malformations, mitral dysplasia, and scoliosis associated with 7q34-q36.3 heterozygous terminal deletion.
Jackson, Carolyn C; Lefèvre-Utile, Alain; Guimier, Anne; Malan, Valérie; Bruneau, Julie; Gessain, Antoine; Cassar, Olivier; Amiel, Jeanne; Cobat, Aurélie; Rattina, Vimel; Abel, Laurent; Casanova, Jean-Laurent; Blanche, Stéphane.
Afiliação
  • Jackson CC; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, New York.
  • Lefèvre-Utile A; Department of Pediatrics, The Memorial Sloan Kettering Cancer Center, New York, New York.
  • Guimier A; Division of Pediatric Hematology/Oncology, Weill Cornell Medical Center, New York, New York.
  • Malan V; Pediatric Immunology-Hematology-Rheumatology Unit, Necker-Enfants Malades Hospital, Paris, France.
  • Bruneau J; Department of Genetics, Necker-Enfants Malades Hospital, AP-HP, Paris, France.
  • Gessain A; Department of Genetics, Necker-Enfants Malades Hospital, AP-HP, Paris, France.
  • Cassar O; Unit of Pathology, Necker-Enfants Malades Hospital, Paris, France.
  • Amiel J; Unit of Epidemiology and Physiopathology of Oncogenic Viruses, Pasteur Institute, Paris, France.
  • Cobat A; Unit of Epidemiology and Physiopathology of Oncogenic Viruses, Pasteur Institute, Paris, France.
  • Rattina V; Department of Genetics, Necker-Enfants Malades Hospital, AP-HP, Paris, France.
  • Abel L; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Necker-Enfants Malades Hospital, INSERM, Paris, France.
  • Casanova JL; Paris Descartes University, Imagine Institute, Paris, France.
  • Blanche S; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Necker-Enfants Malades Hospital, INSERM, Paris, France.
Am J Med Genet A ; 173(7): 1858-1865, 2017 Jul.
Article em En | MEDLINE | ID: mdl-28488400
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.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article