Literature DB >> 16295028

Hemophilia: a practical approach to genetic testing.

Rajiv K Pruthi1.   

Abstract

Hemophilia and von Willebrand disease together account for the large majority of congenital bleeding disorders. Contemporary management, including development of safer clotting factor concentrates and increased emphasis on long-term follow-up in comprehensive hemophilia centers, has improved both quality of life and longevity for patients with congenital bleeding disorders. In addition to facilitating development of recombinant clotting factor concentrates, isolation and characterization of the respective genes have led to increasing availability of a repertoire of genetic tests that, although expensive, are critical for appropriate genetic counseling of affected patients and their family members. This article provides a practical approach to using genetic testing for hemophilia A and B.

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Year:  2005        PMID: 16295028     DOI: 10.4065/80.11.1485

Source DB:  PubMed          Journal:  Mayo Clin Proc        ISSN: 0025-6196            Impact factor:   7.616


  3 in total

1.  Accurate, simple, and inexpensive assays to diagnose F8 gene inversion mutations in hemophilia A patients and carriers.

Authors:  Debargh Dutta; Devi Gunasekera; Margaret V Ragni; Kathleen P Pratt
Journal:  Blood Adv       Date:  2016-12-14

2.  Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM.

Authors:  Shin-Yu Lin; Yi-Ning Su; Chia-Cheng Hung; Woei Tsay; Shyh-Shin Chiou; Chieh-Ting Chang; Hong-Nerng Ho; Chien-Nan Lee
Journal:  BMC Med Genet       Date:  2008-06-20       Impact factor: 2.103

3.  One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementation.

Authors:  Stephen E Lincoln; Tina Hambuch; Justin M Zook; Sara L Bristow; Kathryn Hatchell; Rebecca Truty; Michael Kennemer; Brian H Shirts; Andrew Fellowes; Shimul Chowdhury; Eric W Klee; Shazia Mahamdallie; Megan H Cleveland; Peter M Vallone; Yan Ding; Sheila Seal; Wasanthi DeSilva; Farol L Tomson; Catherine Huang; Russell K Garlick; Nazneen Rahman; Marc Salit; Stephen F Kingsmore; Matthew J Ferber; Swaroop Aradhya; Robert L Nussbaum
Journal:  Genet Med       Date:  2021-05-18       Impact factor: 8.822

  3 in total

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