Literature DB >> 1211959

Comparison of an amino acid mixture and protein hydrolysates in treatment of infants with phenylketonuria.

I Smith, D E Francis, B E Clayton, O H Wolff.   

Abstract

This study compares three feeding regimens for infants with phenylketonuria diagnosed by neonatal screening. Group 1 (five children) received Minafen (Cow & Gate) until they weighed twice their birthweights; Aminogran (Allen & Hanbury) was then added to the feeds in increasing amounts and replaced Minafen at between 8 and 10 months of age. Group 2 (five children) received Aminogran from the neonatal period. Group 3 (five children) received Minafen until they weighed twice their birthweights; Cymogran (Allen & Hanbury) was then added in increasing amounts and replaced Minafen at between 8 and 10 months of age. In all three groups growth was normal and control of phenylalanine levels satisfactory. During the first few months of life the Aminogran regimen proved more complicated and caused more practical difficulties than the regimens starting with Minafen. Later in the first year, when mixed feeding was introduced, and particularly when the bottle was exchanged for the cup, Aminogran had advantages over Cymogran because of its low calorie content, small bulk, and less unpleasant taste. At this age feeding problems were fewer and easier to manage with Aminogran than with Cymogran. A method of using Aminogran in the management of such problems is described. For these reasons, the regimen fed group 1, in which Minafen is used initially and then replaced by Aminogran, is preferred to the other two.

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Year:  1975        PMID: 1211959      PMCID: PMC1545739          DOI: 10.1136/adc.50.11.864

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  6 in total

1.  A METHOD FOR FEEDING THE PHENYLKETONURIC INFANT.

Authors:  B CLAYTON; D FRANCIS; A MONCRIEFF
Journal:  Br Med J       Date:  1965-01-02

2.  THE BLUE DIAPER SYNDROME: FAMILIAL HYPERCALCEMIA WITH NEPHROCALCINOSIS AND INDICANURIA; A NEW FAMILIAL DISEASE, WITH DEFINITION OF THE METABOLIC ABNORMALITY.

Authors:  K N DRUMMOND; A F MICHAEL; R A ULSTROM; R A GOOD
Journal:  Am J Med       Date:  1964-12       Impact factor: 4.965

3.  Mineral and trace-metal balances in children receiving normal and synthetic diets.

Authors:  F W Alexander; B E Clayton; H T Delves
Journal:  Q J Med       Date:  1974-01

4.  The effect of protein loads on plasma amino acid levels.

Authors:  T Palmer; M A Rossiter; B Levin; V G Oberholzer
Journal:  Clin Sci Mol Med       Date:  1973-12

5.  The plasma aminogram. I. Influence of the level of protein intake and a comparison of whole protein and amino acid diets.

Authors:  S E Snyderman; L E Holt; P M Nortn; E Roitman; S V Phansalkar
Journal:  Pediatr Res       Date:  1968-03       Impact factor: 3.756

6.  Use of an amino acid mixture in treatment of phenylketonuria.

Authors:  A Bentovim; B E Clayton; D E Francis; J Shepherd; O H Wolff
Journal:  Arch Dis Child       Date:  1970-10       Impact factor: 3.791

  6 in total

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