Literature DB >> 6629607

Pseudoscleroderma and phenylketonuria.

G Y Guillet, N Dore, J P Hehunstre, J Maleville, J Battin.   

Abstract

An infant girl with partial phenylketonuria developed pseudoscleroderma. After six years of follow up, both the neurologic and cutaneous conditions improved under a phenylalanine restricted diet. The probable roles of phenylalanine, tryptophan, tyrosine, and their metabolites may cause both conditions through possible transient hypersensitivity of cutaneous and muscular tissues.

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Year:  1983        PMID: 6629607     DOI: 10.1111/j.1365-4362.1983.tb02163.x

Source DB:  PubMed          Journal:  Int J Dermatol        ISSN: 0011-9059            Impact factor:   2.736


  2 in total

1.  Phenylketonuria and scleroderma.

Authors:  E H Brown; H K Berry; J Olson; J Levinson
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

2.  Progressive systemic scleroderma in an infant with partial phenylketonuria.

Authors:  M Haktan; A Aydin; H Bahat; B Tuysuz; H Yazici; S Altay
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

  2 in total

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