Literature DB >> 7091578

Sickle cell disease in childhood. Strategies for early diagnosis.

V E Headings.   

Abstract

Early diagnosis of hemoglobin diseases means the identification of a molecular phenotype at a stage when there is opportunity to prevent, minimize, or more adequately adapt to an anticipated health burden. Such diagnosis is presently possible in early childhood, in the neonatal stage, and in fetal stage. A benefit of early diagnosis at all of these stages is the provision of additional options to parents for making informed decisions regarding prevention or for coping with the anticipated hemoglobin disease.

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Year:  1982        PMID: 7091578

Source DB:  PubMed          Journal:  Am J Pediatr Hematol Oncol        ISSN: 0192-8562


  4 in total

Review 1.  Sickle cell states and the anaesthetist.

Authors:  D W Esseltine; M R Baxter; J C Bevan
Journal:  Can J Anaesth       Date:  1988-07       Impact factor: 5.063

2.  Newborn screening: a potpourri of policies.

Authors:  P L Townes
Journal:  Am J Public Health       Date:  1986-10       Impact factor: 9.308

3.  Newborn screening for hemoglobinopathies: the benefit beyond the target.

Authors:  R Grover; S Newman; D Wethers; K Anyane-Yeboa; K Pass
Journal:  Am J Public Health       Date:  1986-10       Impact factor: 9.308

4.  HemoTypeSC point-of-care testing shows high sensitivity with alkaline cellulose acetate hemoglobin electrophoresis for screening hemoglobin SS and SC genotypes.

Authors:  Samuel Ademola Adegoke; Oluwatoyin Ibukun Oladimeji; Morenike Agnes Akinlosotu; Alex Ifeoluwa Akinwumi; Kayode Ademola Matthew
Journal:  Hematol Transfus Cell Ther       Date:  2021-01-27
  4 in total

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