Literature DB >> 24888387

Inherited bone marrow failure syndromes in adolescents and young adults.

David B Wilson1, Daniel C Link, Philip J Mason, Monica Bessler.   

Abstract

The inherited bone marrow failure syndromes are a diverse group of genetic diseases associated with inadequate production of one or more blood cell lineages. Examples include Fanconi anemia, dyskeratosis congenita, Diamond-Blackfan anemia, thrombocytopenia absent radii syndrome, severe congenital neutropenia, and Shwachman-Diamond syndrome. The management of these disorders was once the exclusive domain of pediatric subspecialists, but increasingly physicians who care for adults are being called upon to diagnose or treat these conditions. Through a series of patient vignettes, we highlight the clinical manifestations of inherited bone marrow failure syndromes in adolescents and young adults. The diagnostic and therapeutic challenges posed by these diseases are discussed.

Entities:  

Keywords:  Diamond–Blackfan anemia; Fanconi anemia; Shwachman–Diamond syndrome; aplastic anemia; congenital neutropenia; dyskeratosis congenita; myelodysplastic syndromes; thrombocytopenia absent radii syndrome

Mesh:

Year:  2014        PMID: 24888387      PMCID: PMC4426964          DOI: 10.3109/07853890.2014.915579

Source DB:  PubMed          Journal:  Ann Med        ISSN: 0785-3890            Impact factor:   4.709


  99 in total

1.  Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study.

Authors:  Blanche P Alter; Neelam Giri; Sharon A Savage; June A Peters; Jennifer T Loud; Lisa Leathwood; Ann G Carr; Mark H Greene; Philip S Rosenberg
Journal:  Br J Haematol       Date:  2010-04-30       Impact factor: 6.998

2.  Dysfunctional telomeres and dyskeratosis congenita.

Authors:  Monica Bessler; Hong-Yan Du; Baiwei Gu; Philip J Mason
Journal:  Haematologica       Date:  2007-08       Impact factor: 9.941

3.  TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements.

Authors:  Hong-Yan Du; Elena Pumbo; Jennifer Ivanovich; Ping An; Richard T Maziarz; Ulrike M Reiss; Deborah Chirnomas; Akiko Shimamura; Adrianna Vlachos; Jeffrey M Lipton; Rakesh K Goyal; Frederick Goldman; David B Wilson; Philip J Mason; Monica Bessler
Journal:  Blood       Date:  2008-10-17       Impact factor: 22.113

4.  Dyskeratosis congenita: oral hyperkeratosis in association with lichenoid reaction.

Authors:  T P B Handley; G R Ogden
Journal:  J Oral Pathol Med       Date:  2006-09       Impact factor: 4.253

5.  Shwachman-Diamond syndrome: An inherited preleukemic bone marrow failure disorder with aberrant hematopoietic progenitors and faulty marrow microenvironment.

Authors:  Y Dror; M H Freedman
Journal:  Blood       Date:  1999-11-01       Impact factor: 22.113

Review 6.  Pathophysiology and management of inherited bone marrow failure syndromes.

Authors:  Akiko Shimamura; Blanche P Alter
Journal:  Blood Rev       Date:  2010-04-24       Impact factor: 8.250

Review 7.  In vivo reversion to normal of inherited mutations in humans.

Authors:  R Hirschhorn
Journal:  J Med Genet       Date:  2003-10       Impact factor: 6.318

8.  The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy.

Authors:  Philip S Rosenberg; Blanche P Alter; Audrey A Bolyard; Mary Ann Bonilla; Laurence A Boxer; Bonnie Cham; Carol Fier; Melvin Freedman; George Kannourakis; Sally Kinsey; Beate Schwinzer; Connie Zeidler; Karl Welte; David C Dale
Journal:  Blood       Date:  2006-02-23       Impact factor: 22.113

9.  Mutations in neutrophil elastase causing congenital neutropenia lead to cytoplasmic protein accumulation and induction of the unfolded protein response.

Authors:  Inga Köllner; Beate Sodeik; Sabine Schreek; Holger Heyn; Nils von Neuhoff; Manuela Germeshausen; Cornelia Zeidler; Martin Krüger; Brigitte Schlegelberger; Karl Welte; Carmela Beger
Journal:  Blood       Date:  2006-03-21       Impact factor: 22.113

10.  Diagnosis of fanconi anemia: chromosomal breakage analysis.

Authors:  Anneke B Oostra; Aggie W M Nieuwint; Hans Joenje; Johan P de Winter
Journal:  Anemia       Date:  2012-05-24
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  23 in total

1.  Genetic predisposition to myelodysplastic syndrome and acute myeloid leukemia in children and young adults.

Authors:  Daria V Babushok; Monica Bessler; Timothy S Olson
Journal:  Leuk Lymphoma       Date:  2015-12-23

Review 2.  Diagnosis and Treatment of Aplastic Anemia.

Authors:  Scott A Peslak; Timothy Olson; Daria V Babushok
Journal:  Curr Treat Options Oncol       Date:  2017-11-16

3.  Postvaccination graft dysfunction/aplastic anemia relapse with massive clonal expansion of autologous CD8+ lymphocytes.

Authors:  Caitlin Ritz; Wenzhao Meng; Natasha L Stanley; Miren L Baroja; Chong Xu; Patrick Yan; Alexander C Huang; Ryan Hausler; Peter Nicholas; Jian-Meng Fan; David Lieberman; Beatriz M Carreno; Eline T Luning Prak; Timothy S Olson; Daria V Babushok
Journal:  Blood Adv       Date:  2020-04-14

Review 4.  Modeling Human Bone Marrow Failure Syndromes Using Pluripotent Stem Cells and Genome Engineering.

Authors:  Moonjung Jung; Cynthia E Dunbar; Thomas Winkler
Journal:  Mol Ther       Date:  2015-10-05       Impact factor: 11.454

Review 5.  Old and new tools in the clinical diagnosis of inherited bone marrow failure syndromes.

Authors:  Allison H West; Jane E Churpek
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

Review 6.  Radiographic assessment of congenital malformations of the upper extremity.

Authors:  Matthew J Winfeld; Hansel Otero
Journal:  Pediatr Radiol       Date:  2016-06-15

7.  Idiopathic aplastic anemia vs hypocellular myelodysplastic syndrome.

Authors:  Jibran Durrani; Jaroslaw P Maciejewski
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2019-12-06

Review 8.  The genetics of myelodysplastic syndrome: from clonal haematopoiesis to secondary leukaemia.

Authors:  Adam S Sperling; Christopher J Gibson; Benjamin L Ebert
Journal:  Nat Rev Cancer       Date:  2016-11-11       Impact factor: 60.716

9.  Why is an energy metabolic defect the common outcome in BMFS?

Authors:  Paolo Degan; Silvia Ravera; Enrico Cappelli
Journal:  Cell Cycle       Date:  2016-08-11       Impact factor: 4.534

10.  Fanconi Anemia Mesenchymal Stromal Cells-Derived Glycerophospholipids Skew Hematopoietic Stem Cell Differentiation Through Toll-Like Receptor Signaling.

Authors:  Surya Amarachintha; Mathieu Sertorio; Andrew Wilson; Xiaoli Li; Qishen Pang
Journal:  Stem Cells       Date:  2015-07-24       Impact factor: 6.277

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