Bleeding disorders in Noonan syndrome

Benjamin J. Briggs*, Joseph D. Dickerman

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

47 Scopus citations

Abstract

Noonan Syndrome (NS) is a common genetic disease with multiple organ defects including bleeding disorders, which was last reviewed in 1997. Since then significant information has been acquired regarding bleeding problems in NS, specifically on the underlying genetics. Associations between mutated genes and bleeding disorders are reviewed along with prevalence and underlying etiologies. Between 50-89% of NS patients will have a bleeding disorder and since a significant number will require surgery it is important to identify which ones are at risk prior to their procedure. Recommendations regarding screening for bleeding disorders and their treatment are discussed.

Original languageEnglish
Pages (from-to)167-172
Number of pages6
JournalPediatric Blood and Cancer
Volume58
Issue number2
DOIs
StatePublished - Feb 2012

Keywords

  • Bleeding disorders
  • Genetics
  • Hemostasis
  • Neurocardiofacialcutaneous syndrome family
  • Noonan syndrome

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