Literature DB >> 19167578

Congenital cytopenias and bone marrow failure syndromes.

Angela Rivers1, William B Slayton.   

Abstract

Congenital bone marrow failure syndromes (CBMFS) are extremely uncommon diseases that can present in the neonate. The objective of this article is to review the presentation, diagnosis, pathophysiology, and management of CBMFS in relation to neonatology. CBMFS should be considered when a single or multiple blood cell lineages are low secondary to failure of production. Diagnosis in the neonatal period requires a high index of suspicion. In this particular age group, CBMFS should be considered when the neonate has a family history of CBMFS, is small for gestational age, or has other physical abnormalities. History and physical examination can lead to the diagnosis. CBMFS are often associated with a predisposition to cancer later in life.

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Year:  2009        PMID: 19167578     DOI: 10.1053/j.semperi.2008.10.009

Source DB:  PubMed          Journal:  Semin Perinatol        ISSN: 0146-0005            Impact factor:   3.300


  3 in total

Review 1.  Neonatal manifestations of inherited bone marrow failure syndromes.

Authors:  Payal P Khincha; Sharon A Savage
Journal:  Semin Fetal Neonatal Med       Date:  2015-12-24       Impact factor: 3.926

2.  Approach to neonatal thrombocytopenia: immature platelet fraction has a major role.

Authors:  Jyoti Kotwal
Journal:  Med J Armed Forces India       Date:  2011-08-07

3.  CAMT-MPL: congenital amegakaryocytic thrombocytopenia caused by MPL mutations - heterogeneity of a monogenic disorder - a comprehensive analysis of 56 patients.

Authors:  Manuela Germeshausen; Matthias Ballmaier
Journal:  Haematologica       Date:  2021-09-01       Impact factor: 9.941

  3 in total

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