Literature DB >> 25377322

Historical review on genetic analysis in hemophilia A.

Johannes Oldenburg1, Behnaz Pezeshkpoor1, Anna Pavlova1.   

Abstract

Molecular genetic analysis is widely applied in inherited bleeding disorders. The outcome of genetic analysis allows genetic counselling in affected families and helps to find a link between the genotype and phenotype. Genetic analysis in hemophilia A (HA) has tremendously improved in the past decades. Many new techniques and modifications as well as analysis software have become available, which has enabled genetic analysis and interpretation of data to become faster and more accurate. The advances in mutation detection strategies facilitate the identification of the causal mutation in up to 97% of patients with HA. This review discusses the milestones in genetic analysis of HA and highlights the importance of identification of the causative mutations for genetic counseling and particularly for the interpretation of the clinical presentation of HA patients. Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

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Year:  2014        PMID: 25377322     DOI: 10.1055/s-0034-1395161

Source DB:  PubMed          Journal:  Semin Thromb Hemost        ISSN: 0094-6176            Impact factor:   4.180


  6 in total

Review 1.  Diagnosis and care of patients with mild haemophilia: practical recommendations for clinical management.

Authors:  Gary Benson; Günter Auerswald; Gerry Dolan; Anne Duffy; Cedric Hermans; Rolf Ljung; Massimo Morfini; Silva Zupančić Šalek
Journal:  Blood Transfus       Date:  2017-11-14       Impact factor: 3.443

2.  Demonstration of a novel Xp22.2 microdeletion as the cause of familial extreme skewing of X-inactivation utilizing case-parent trio SNP microarray analysis.

Authors:  Jane A Mason; Hnin T Aung; Adayapalam Nandini; Rickie G Woods; David J Fairbairn; John A Rowell; David Young; Rachel D Susman; Simon A Brown; Valentine J Hyland; Jeremy D Robertson
Journal:  Mol Genet Genomic Med       Date:  2018-02-28       Impact factor: 2.183

3.  Application of Indirect Linkage Analysis for Carrier Detection of Hemophilia A in Kurdistan Region of Iraq: Usefulness of Intron 18 BclI T>A, Intron 19 HindIII C>T, and IVS7 nt27 G>A Markers.

Authors:  Aveen M Raouf Abdulqader; Shwan Rachid; Ali Ibrahim Mohammed; Sarwar Noori Mahmood
Journal:  Clin Appl Thromb Hemost       Date:  2019 Jan-Dec       Impact factor: 2.389

Review 4.  Prevalence of symptoms in hemophilia carriers in comparison with the general population: a systematic review.

Authors:  André Bubna Hirayama; Alline Karolyne Cândida da Silva; Jordanna Sousa Rocha; Maria do Rosário Ferraz Roberti
Journal:  Hematol Transfus Cell Ther       Date:  2019-06-17

5.  Correction of a Factor VIII genomic inversion with designer-recombinases.

Authors:  Felix Lansing; Liliya Mukhametzyanova; Teresa Rojo-Romanos; Kentaro Iwasawa; Masaki Kimura; Maciej Paszkowski-Rogacz; Janet Karpinski; Tobias Grass; Jan Sonntag; Paul Martin Schneider; Ceren Günes; Jenna Hoersten; Lukas Theo Schmitt; Natalia Rodriguez-Muela; Ralf Knöfler; Takanori Takebe; Frank Buchholz
Journal:  Nat Commun       Date:  2022-01-20       Impact factor: 14.919

6.  Pairing of single mutations yields obligate Cre-type site-specific recombinases.

Authors:  Jenna Hoersten; Gloria Ruiz-Gómez; Felix Lansing; Teresa Rojo-Romanos; Lukas Theo Schmitt; Jan Sonntag; M Teresa Pisabarro; Frank Buchholz
Journal:  Nucleic Acids Res       Date:  2022-01-25       Impact factor: 16.971

  6 in total

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