Prolidase and prolidase deficiency.

Abstract:

:Prolidase deficiency seems to be a rather rare metabolic disorder. However, many new cases can be detected because screening is easy to perform and enzymatic confirmation allows the differentiation from other iminodipeptidurias . Clinical symptoms are briefly reviewed, while biological considerations and prolidase properties are exhaustively described. Methods for investigating urinary iminodipeptides are given with results. Moreover, several collagen modifications observed in this disorder led us to formulate a hypothesis for their mechanism. Genetic considerations and treatment attempts are discussed.

journal_name

Life Sci

journal_title

Life sciences

authors

Myara I,Charpentier C,Lemonnier A

doi

10.1016/0024-3205(84)90363-1

subject

Has Abstract

pub_date

1984-05-21 00:00:00

pages

1985-98

issue

21

eissn

0024-3205

issn

1879-0631

pii

0024-3205(84)90363-1

journal_volume

34

pub_type

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