Literature DB >> 15662710

Prenatal diagnosis of Fanconi anemia (Group C) subsequent to abnormal sonographic findings.

Amy Merrill1, Lynne Rosenblum-Vos, Deborah A Driscoll, Katherine Daley, Karen Treat.   

Abstract

Manifestations of Fanconi Anemia Complementation Group C (FA-C) include multiple major congenital malformations, hypoplastic radius, absent thumb, growth retardation, elfin-like facial features, microphthalmia, microcephaly, cafe-au-lait spots, early onset of hematologic disease and poor survival (Auerbach, 1997). We describe two cases in which second-trimester sonographic findings led to parental carrier testing for FA-C and subsequent prenatal diagnosis of affected fetuses. Copyright (c) 2005 John Wiley & Sons, Ltd.

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Year:  2005        PMID: 15662710     DOI: 10.1002/pd.1055

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  2 in total

1.  Pregnancy outcomes in mothers of offspring with inherited bone marrow failure syndromes.

Authors:  Neelam Giri; Helen D Reed; Pamela Stratton; Sharon A Savage; Blanche P Alter
Journal:  Pediatr Blood Cancer       Date:  2017-08-12       Impact factor: 3.167

2.  Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing.

Authors:  Johan J P Gille; Karijn Floor; Lianne Kerkhoven; Najim Ameziane; Hans Joenje; Johan P de Winter
Journal:  Anemia       Date:  2012-06-21
  2 in total

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