Literature DB >> 22012616

Bleeding disorders in Noonan syndrome.

Benjamin J Briggs1, Joseph D Dickerman.   

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.
Copyright © 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 22012616     DOI: 10.1002/pbc.23358

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  8 in total

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Review 5.  Advances in the Understanding of the Genetic Determinants of Congenital Heart Disease and Their Impact on Clinical Outcomes.

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6.  Evaluation of bleeding disorders in patients with Noonan syndrome: a systematic review.

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Journal:  Orphanet J Rare Dis       Date:  2021-12-02       Impact factor: 4.123

8.  Prolonged thrombocytopenia in a neonate with Noonan syndrome: a case report.

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  8 in total

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