Literature DB >> 402512

Erythrocyte morphology in genetic defects of the Rh and Kell blood group systems.

H F Taswell, J C Lewis, W L Marsh, B M Wimer, A A Pineda, S M Brzica.   

Abstract

Absence of KX antigen and of normal expression of the Kell system antigens is associated with bizarre red blood cell morphology when observed by either light or scanning electron microscopy. Numerous acanthocytes and dacryocytes have been observed in the peripheral blood smear of an apparently healthy individual with McLeod-phenotype blood, in a male patient with type II chronic granulomatous disease who had a shortened 51Cr red blood cell survival time, and in a minor population of the red blood cells of his carrier mother.

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Year:  1977        PMID: 402512

Source DB:  PubMed          Journal:  Mayo Clin Proc        ISSN: 0025-6196            Impact factor:   7.616


  2 in total

1.  [Rhnull syndrome in two female siblings from Pakistan (author's transl)].

Authors:  W Weise; L Ballowitz; W Martin
Journal:  Blut       Date:  1981-10

2.  Chronic granulomatous disease, the McLeod phenotype and the contiguous gene deletion syndrome-a review.

Authors:  Casey E Watkins; John Litchfield; Eunkyung Song; Gayatri B Jaishankar; Niva Misra; Nikhil Holla; Michelle Duffourc; Guha Krishnaswamy
Journal:  Clin Mol Allergy       Date:  2011-11-23
  2 in total

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