Mayo Clin Proc. 1977 Mar;52(3):157-9.

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

Taswell HF, Lewis JC, Marsh WL, Wimer BM, Pineda AA, Brzica SM Jr.

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.

PMID:: 402512; [PubMed - indexed for MEDLINE]

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Hereditary acanthocytosis associated with the McLeod phenotype of the Kell blood group system. [Br J Haematol. 1979]
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Symmans WA, Shepherd CS, Marsh WL, Oyen R, Shohet SB, Linehan BJ. Br J Haematol. 1979 Aug; 42(4):575-83.
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Cited by 1 PubMed Central article

Chronic granulomatous disease, the McLeod phenotype and the contiguous gene deletion syndrome-a review. [Clin Mol Allergy. 2011]
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