Literature DB >> 23815883

Velopharyngeal insufficiency, submucous cleft palate and a phonological disorder as the associated clinical features which led to the diagnosis of Jacobsen syndrome. Case report and review of the literature.

Antonio Ysunza1, Kenneth Shaheen, David J Aughton, Mark A Micale, Richard Merson, Kris Rutkowski.   

Abstract

Jacobsen syndrome is an uncommon but well-known contiguous gene syndrome caused by partial deletion involving the long arm of chromosome 11. Most common features include: psychomotor impairment, facial dysmorphism, and thrombocytopenia. Cleft palate has been rarely reported. A case of Jacobsen syndrome confirmed by cytogenomic analysis is presented with review of the literature. Main clinical features were phonological disorder, submucous cleft palate (SMCP) and velopharyngeal insufficiency (VPI). VPI was corrected surgically according to findings of videonasopharyngoscopy and videofluoroscopy. It is concluded that clinicians should consider that VPI associated with SMCP may be the main manifestations of a chromosomal syndrome.
Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Cleft palate; Jacobsen syndrome; Speech; Surgery

Mesh:

Year:  2013        PMID: 23815883     DOI: 10.1016/j.ijporl.2013.06.007

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  2 in total

1.  Ventriculomegaly and cerebellar hypoplasia in a neonate with interstitial 11q 24 deletion in Jacobsen syndrome region.

Authors:  Surasak Puvabanditsin; Charlotte Wang Chen; Marissa Botwinick; Karen Hussein; Joseph Mariduena; Rajeev Mehta
Journal:  Clin Case Rep       Date:  2018-05-22

Review 2.  Ultrasonographic findings and prenatal diagnosis of Jacobsen syndrome: A case report and review of the literature.

Authors:  Shuang Chen; Ruixue Wang; Xinyue Zhang; Leilei Li; Yuting Jiang; Ruizhi Liu; Hongguo Zhang
Journal:  Medicine (Baltimore)       Date:  2020-01       Impact factor: 1.817

  2 in total

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