Literature DB >> 28168417

First case report of hemophilia B Leyden in Japan.

Atsuki Yamashita1, Chiai Nagae2, Mika Mori3, Tomoko Ashikaga2, Tetsuhito Kojima4, Masashi Taki3.   

Abstract

Hemophilia B Leyden is a unique subtype of hemophilia B, characterized by increasing factor IX activity (FIX:C) after puberty and a lower normal range of FIX:C throughout adulthood. However, to date, no Japanese case has been reported. Here, we report a case of hemophilia B Leyden in a 22-year-old male. He suffered from subgaleal hematoma, and was subsequently diagnosed with hemophilia B (FIX:C 0.2%) in the neonatal period. Both his parents are Japanese. There was no history of hemophilia in his family. FIX:C gradually increased with age (8% at age = 1; 14% at age = 7; 19% at age = 12; 32% at age = 18). FIX:C is within the range 30-40% in recent several years. He once required administration of FIX concentrate against traumatic tongue bleeding at 7 years of age. Genotyping analysis of FIX was performed after informed consent at 21 years of age, and a point mutation (c.-35G>A) was detected. This mutation has been reported previously as the Leyden mutation. Although it has been reported that hemophilia B Leyden is seen in 1.9% of patients with hemophilia B, the present case is the first report of hemophilia B Leyden from Japan.

Entities:  

Keywords:  Hemophilia B; Japanese; Leyden mutation

Mesh:

Substances:

Year:  2017        PMID: 28168417     DOI: 10.1007/s12185-017-2194-4

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  10 in total

1.  An age-related homeostasis mechanism is essential for spontaneous amelioration of hemophilia B Leyden.

Authors:  Sumiko Kurachi; Jeffrey S Huo; Afshin Ameri; Kezhong Zhang; Akiyasu C Yoshizawa; Kotoku Kurachi
Journal:  Proc Natl Acad Sci U S A       Date:  2009-04-28       Impact factor: 11.205

2.  Haemophilia B Brandenberg-type promoter mutation.

Authors:  J A Heit; R P Ketterling; R E Zapata; S M Ordonez; C K Kasper; S S Sommer
Journal:  Haemophilia       Date:  1999-01       Impact factor: 4.287

3.  Recovery from hemophilia B Leyden: an androgen-responsive element in the factor IX promoter.

Authors:  M Crossley; M Ludwig; K M Stowell; P De Vos; K Olek; G G Brownlee
Journal:  Science       Date:  1992-07-17       Impact factor: 47.728

4.  Assessment of the F9 genotype-specific FIX inhibitor risks and characterisation of 10 novel severe F9 defects in the first molecular series of Argentinian patients with haemophilia B.

Authors:  Claudia Pamela Radic; Liliana Carmen Rossetti; Miguel Martín Abelleyro; Miguel Candela; Raúl Pérez Bianco; Miguel de Tezanos Pinto; Irene Beatriz Larripa; Anne Goodeve; Carlos Daniel De Brasi
Journal:  Thromb Haemost       Date:  2012-10-23       Impact factor: 5.249

5.  An interactive mutation database for human coagulation factor IX provides novel insights into the phenotypes and genetics of hemophilia B.

Authors:  P M Rallapalli; G Kemball-Cook; E G Tuddenham; K Gomez; S J Perkins
Journal:  J Thromb Haemost       Date:  2013-07       Impact factor: 5.824

6.  Monoclonal B-cell lymphocytosis is characterized by mutations in CLL putative driver genes and clonal heterogeneity many years before disease progression.

Authors:  J Ojha; C Secreto; K Rabe; J Ayres-Silva; R Tschumper; D V Dyke; S Slager; R Fonseca; T Shanafelt; N Kay; E Braggio
Journal:  Leukemia       Date:  2014-07-18       Impact factor: 11.528

7.  Another genetic variant of haemophilia B: haemophilia B Leyden.

Authors:  J J Veltkamp; J Meilof; H G Remmelts; D van der Vlerk; E A Loeliger
Journal:  Scand J Haematol       Date:  1970

Review 8.  Hemophilia B Leyden and once mysterious cis-regulatory mutations.

Authors:  Alister P W Funnell; Merlin Crossley
Journal:  Trends Genet       Date:  2013-10-16       Impact factor: 11.639

Review 9.  Hemophilia B: molecular pathogenesis and mutation analysis.

Authors:  A C Goodeve
Journal:  J Thromb Haemost       Date:  2015-05-18       Impact factor: 5.824

10.  A CpG mutational hotspot in a ONECUT binding site accounts for the prevalent variant of hemophilia B Leyden.

Authors:  Alister P W Funnell; Michael D Wilson; Benoit Ballester; Ka Sin Mak; Jon Burdach; Natisha Magan; Richard C M Pearson; Frederic P Lemaigre; Kathryn M Stowell; Duncan T Odom; Paul Flicek; Merlin Crossley
Journal:  Am J Hum Genet       Date:  2013-03-07       Impact factor: 11.025

  10 in total

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