Literature DB >> 1392398

Congenital sideroblastic anaemia with intrauterine symptoms and early lethal outcome.

K Andersen1, P H Kaad.   

Abstract

Sideroblastic anaemia is a rare disease, which most often presents in early childhood. A case of ringed sideroblastic anaemia with onset in early foetal life in a female infant, resulting in severe intrauterine symptoms, is reported. Six weeks after birth a bone marrow examination revealed a large amount of typical ringed sideroblasts, thus establishing the diagnosis. In spite of repeated blood transfusions, the haemoglobin content gradually decreased. The condition was refractory to pyridoxal phosphate treatment and continued to deteriorate with lethal outcome four months after birth.

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Year:  1992        PMID: 1392398     DOI: 10.1111/j.1651-2227.1992.tb12324.x

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  2 in total

Review 1.  X-linked sideroblastic anaemia in a female fetus: a case report and a literature review.

Authors:  Diane Nzelu; Panicos Shangaris; Lisa Story; Frances Smith; Chinthika Piyasena; Jayanthi Alamelu; Amira Elmakky; Maria Pelidis; Rachel Mayhew; Srividhya Sankaran
Journal:  BMC Med Genomics       Date:  2021-12-20       Impact factor: 3.063

Review 2.  Pyridoxine-refractory congenital sideroblastic anaemia with evidence for autosomal inheritance: exclusion of linkage to ALAS2 at Xp11.21 by polymorphism analysis.

Authors:  P E Jardine; P D Cotter; S A Johnson; E J Fitzsimons; L Tyfield; P W Lunt; D F Bishop
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

  2 in total

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