Literature DB >> 28488400

Kaposi sarcoma, oral malformations, mitral dysplasia, and scoliosis associated with 7q34-q36.3 heterozygous terminal deletion.

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.
© 2017 Wiley Periodicals, Inc.

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


  36 in total

1.  Distinct distribution of rare US genotypes of Kaposi's sarcoma-associated herpesvirus (KSHV) in South Texas: implications for KSHV epidemiology.

Authors:  Y J Zhang; T L Davis; X P Wang; J H Deng; J Baillargeon; I T Yeh; H B Jenson; S J Gao
Journal:  J Infect Dis       Date:  2000-11-30       Impact factor: 5.226

2.  Individuals from North America, Australasia, and Africa are infected with four different genotypes of human herpesvirus 8.

Authors:  Y X Meng; T J Spira; G J Bhat; C J Birch; J D Druce; B R Edlin; R Edwards; C Gunthel; R Newton; F R Stamey; C Wood; P E Pellett
Journal:  Virology       Date:  1999-08-15       Impact factor: 3.616

3.  The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.

Authors:  L Nanni; J E Ming; M Bocian; K Steinhaus; D W Bianchi; C Die-Smulders; A Giannotti; K Imaizumi; K L Jones; M D Campo; R A Martin; P Meinecke; M E Pierpont; N H Robin; I D Young; E Roessler; M Muenke
Journal:  Hum Mol Genet       Date:  1999-12       Impact factor: 6.150

Review 4.  To err (meiotically) is human: the genesis of human aneuploidy.

Authors:  T Hassold; P Hunt
Journal:  Nat Rev Genet       Date:  2001-04       Impact factor: 53.242

5.  Terminal deletion of the chromosome 7(q36-qter) in an infant with sacral agenesis and anterior myelomeningocele.

Authors:  Laura Rodríguez; Irene Cuadrado Pérez; Juana Herrera Montes; Maria Luisa Lorente Jareño; Fermina López Grondona; Maria Luisa Martínez-Frías
Journal:  Am J Med Genet       Date:  2002-06-01

6.  HHV-8-associated Kaposi sarcoma in a child with IFNgammaR1 deficiency.

Authors:  Yildiz Camcioglu; Capucine Picard; Vincent Lacoste; Stéphanie Dupuis; Necla Akçakaya; Haluk Cokura; Gültekin Kaner; Cuyan Demirkesen; Sabine Plancoulaine; Jean-François Emile; Antoine Gessain; Jean-Laurent Casanova
Journal:  J Pediatr       Date:  2004-04       Impact factor: 4.406

7.  Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the Sonic Hedgehog gene and the HLXB9 gene at 7q36.3.

Authors:  Denise Horn; Holger Tönnies; Heidemarie Neitzel; Dagmar Wahl; Georg Klaus Hinkel; Arpad von Moers; Oliver Bartsch
Journal:  Am J Med Genet A       Date:  2004-07-01       Impact factor: 2.802

8.  Malignant degeneration of presacral teratoma in the Currarino anomaly.

Authors:  Miguel Urioste; M del Carmen Garcia-Andrade; Laura Valle; Mercedes Robledo; Fernando González-Palacios; Ramiro Méndez; Joaquin Ferreirós; Javier Nuño; Javier Benítez
Journal:  Am J Med Genet A       Date:  2004-07-30       Impact factor: 2.802

9.  Novel mutation in sonic hedgehog in non-syndromic colobomatous microphthalmia.

Authors:  Lisa A Schimmenti; June de la Cruz; Richard Alan Lewis; J D Karkera; Glenda S Manligas; Erich Roessler; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2003-01-30       Impact factor: 2.802

10.  Solitary median maxillary central incisor syndrome: clinical case with a novel mutation of sonic hedgehog.

Authors:  Livia Garavelli; C Zanacca; G Caselli; G Banchini; C Dubourg; V David; S Odent; F Gurrieri; G Neri
Journal:  Am J Med Genet A       Date:  2004-05-15       Impact factor: 2.802

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  3 in total

Review 1.  Clinical, cytogenetic, and molecular findings in a fetus with ultrasonic multiple malformations, 4q duplication, and 7q deletion: A case report and literature review.

Authors:  Fagui Yue; Yuting Jiang; Yang Yu; Xiao Yang; Hongguo Zhang; Ruizhi Liu; Ruixue Wang
Journal:  Medicine (Baltimore)       Date:  2018-11       Impact factor: 1.889

2.  Case Report: Congenital Brain Dysplasia, Developmental Delay and Intellectual Disability in a Patient With a 7q35-7q36.3 Deletion.

Authors:  Liang-Liang Fan; Yue Sheng; Chen-Yu Wang; Ya-Li Li; Ji-Shi Liu
Journal:  Front Genet       Date:  2021-12-01       Impact factor: 4.599

Review 3.  Pathogenesis of infections in HIV-infected individuals: insights from primary immunodeficiencies.

Authors:  Qian Zhang; Pierre Frange; Stéphane Blanche; Jean-Laurent Casanova
Journal:  Curr Opin Immunol       Date:  2017-10-06       Impact factor: 7.486

  3 in total

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