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Cited by 190

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Neonatal Copper Deficiency

Al-Rashid, Rashid A., Spangler, John·1971·New England Journal of Medicine

Abstract

PURE copper deficiency in man has probably never been observed. When it occurs other deficiencies complicate the picture. In infants, a disorder characterized by hypocupremia, hypoferremia, neutropenia, hypoproteinemia and anemia has been reported.1,2Recently, we had the opportunity to study a three-month-old, low-birth-weight infant with the clinical and laboratory picture of copper deficiency who was not marasmic and had been thriving rather well.Case ReportJ.P., a 3-month-old male Indian infant, was referred for evaluation of anemia and a Central-nervous-system disorder. He had been born at 34 weeks' gestation, with an Apgar score of 2 at birth and a weight . . .

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Metadata

Authors
Al-Rashid, R. A., & Spangler, J.
Venue
New England Journal of Medicine
Published
1971-10-07
Volume
285
Issue
15
Pages
841-843
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2086411831
Cited by
190
References
0
FWCI
8.56
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Neonatal Copper Deficiency. https://app.cochat.ai/papers/10.1056/nejm197110072851506
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Al-Rashid, R. A., & Spangler, J. (1971). Neonatal Copper Deficiency. New England Journal of Medicine. https://doi.org/10.1056/nejm197110072851506

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.