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On the screening for inborn errors of galactose metabolism.
Ann Genet. 1983; 26(3):191-2.AG

Abstract

The utility of a simplified diagram of procedures for screening specimens for genetic disorders in galactose metabolism is stressed. Both, early detection and institution of the dietetic treatment are imperative since these inherited disorders have clinical and pathological consequences which can be very severe in galactose-1-phosphate uridyltransferase and uridine diphosphate galactose-4-epimerase deficiencies.

Authors

Vaca G
No affiliation info available
Sànchez-Corona J
No affiliation info available
Olivares N
No affiliation info available
Medina C
No affiliation info available
Ibarra B
No affiliation info available
Cantú JM
No affiliation info available

MeSH

Carbohydrate EpimerasesGalactokinaseGalactosemiasHumansInfant, NewbornMetabolism, Inborn ErrorsUDPglucose 4-EpimeraseUTP-Hexose-1-Phosphate Uridylyltransferase

Pub Type(s)

Journal Article

Language

eng

PubMed ID

6606384

Citation

Vaca, G, et al. "On the Screening for Inborn Errors of Galactose Metabolism." Annales De Genetique, vol. 26, no. 3, 1983, pp. 191-2.
Vaca G, Sànchez-Corona J, Olivares N, et al. On the screening for inborn errors of galactose metabolism. Ann Genet. 1983;26(3):191-2.
Vaca, G., Sànchez-Corona, J., Olivares, N., Medina, C., Ibarra, B., & Cantú, J. M. (1983). On the screening for inborn errors of galactose metabolism. Annales De Genetique, 26(3), 191-2.
Vaca G, et al. On the Screening for Inborn Errors of Galactose Metabolism. Ann Genet. 1983;26(3):191-2. PubMed PMID: 6606384.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - On the screening for inborn errors of galactose metabolism. AU - Vaca,G, AU - Sànchez-Corona,J, AU - Olivares,N, AU - Medina,C, AU - Ibarra,B, AU - Cantú,J M, PY - 1983/1/1/pubmed PY - 1983/1/1/medline PY - 1983/1/1/entrez SP - 191 EP - 2 JF - Annales de genetique JO - Ann Genet VL - 26 IS - 3 N2 - The utility of a simplified diagram of procedures for screening specimens for genetic disorders in galactose metabolism is stressed. Both, early detection and institution of the dietetic treatment are imperative since these inherited disorders have clinical and pathological consequences which can be very severe in galactose-1-phosphate uridyltransferase and uridine diphosphate galactose-4-epimerase deficiencies. SN - 0003-3995 UR - https://www.unboundmedicine.com/medline/citation/6606384/On_the_screening_for_inborn_errors_of_galactose_metabolism_ DB - PRIME DP - Unbound Medicine ER -