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 Scijournal_title
Life sciencesauthors
Myara I,Charpentier C,Lemonnier Adoi
10.1016/0024-3205(84)90363-1subject
Has Abstractpub_date
1984-05-21 00:00:00pages
1985-98issue
21eissn
0024-3205issn
1879-0631pii
0024-3205(84)90363-1journal_volume
34pub_type
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