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Pediatrics. 2001 Dec;108(6):1370-3.

Fatty acids, alpha-fetoprotein, and cystic fibrosis.

Author information

1
Division of Molecular Medicine, Wadsworth Center, Department of Health, Albany, NY 12201, USA. mizejew@wadsworth.org

Abstract

Docosahexaenoic acid, found lacking in animal models of cystic fibrosis, has been proposed as a dietary supplement therapy for this genetic disorder. Alpha-fetoprotein, which binds and transports docosahexaenoic acid, may be a useful marker to improve the management and follow-up in newborn screening programs for cystic fibrosis, because only 20% of such infants are diagnosed at birth.

PMID:
11731663
[Indexed for MEDLINE]

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