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Hemolytic anemia with pyruvate kinase deficiency presenting as paravertebral myelolipoma

✍ Scribed by Schön, H. R. ;Emmerich, B. ;Arnold, H. ;Maubach, P. A. ;Becker, K. ;Rastetter, J.


Publisher
Springer-Verlag
Year
1984
Tongue
English
Weight
938 KB
Volume
62
Category
Article
ISSN
1432-1440

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## Communicated by Mark Paalman Pyruvate kinase (PK) deficiency (PKD) is an autosomal recessive disorder with the typical manifestation of nonspherocytic hemolytic anemia. We analyzed the mutant enzymes of 10 unrelated patients with PKD, whose symptoms ranged from a mild, chronic hemolytic anemia t