Literature DB >> 6790856

Prolidase deficiency with iminodipeptiduria: biochemical investigations and first results of attempted therapy.

C Charpentier, K Dagbovie, A Lemonnier, M Larregue, R A Johnstone.   

Abstract

A 33-year-old female patient with chronic recurrent leg ulcerations was shown to present a massive iminodipeptiduria which seemed to be attributable to disturbance of collagen metabolism. Biochemical investigations confirmed an hereditary prolidase deficiency. A treatment was tried for the first time and showed a good biochemical result and a clinical improvement.

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Year:  1981        PMID： 6790856     DOI： 10.1007/BF02263599

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


  8 in total

1.  An ultramicrotechnique for the detection and separation of small molecular weight peptides from amino acids.

Authors:  H E Gallo-Torres; J Ludorf; O N Miller
Journal:  Anal Biochem       Date:  1975-03       Impact factor: 3.365

2.  Iminopeptiduria, skin ulcerations, and edema in a boy with prolidase deficiency.

Authors:  L J Sheffield; P Schlesinger; K Faull; B J Halpern; G M Schier; R G Cotton; J Hammond; D M Danks
Journal:  J Pediatr       Date:  1977-10       Impact factor: 4.406

3.  A prolidase deficiency in man with iminopeptiduria.

Authors:  G F Powell; M A Rasco; R M Maniscalco
Journal:  Metabolism       Date:  1974-06       Impact factor: 8.694

4.  Further studies on a patient with iminodipeptiduria: a probable case of prolidase deficiency.

Authors:  N R Buist; J J Strandholm; J F Bellinger; N G Kennaway
Journal:  Metabolism       Date:  1972-12       Impact factor: 8.694

5.  A syndrome resembling lathyrism associated with iminodipeptiduria.

Authors:  S I Goodman; C C Solomons; F Muschenheim; C A McIntyre; B Miles; D O'Brien
Journal:  Am J Med       Date:  1968-07       Impact factor: 4.965

6.  Iminodipeptiduria: a genetic defect in recycling collagen; a method for determining prolidase in erythrocytes.

Authors:  S H Jackson; A W Dennis; M Greenberg
Journal:  Can Med Assoc J       Date:  1975-10-18       Impact factor: 8.262

7.  Prolidase deficiency: its dermatological manifestations and some additional biochemical studies.

Authors:  J Arata; S Umemura; Y Yamamoto; M Hagiyama; N Nohara
Journal:  Arch Dermatol       Date:  1979-01

8.  Prolidase deficiency with imidodipeptiduria. A familial case with and without clinical symptoms.

Authors:  M Isemura; T Hanyu; F Gejyo; R Nakazawa; R Igarashi; S Matsuo; K Ikeda; Y Sato
Journal:  Clin Chim Acta       Date:  1979-05-02       Impact factor: 3.786
  8 in total
  6 in total

1.  An autopsy case of prolidase deficiency.

Authors:  M Sekiya; Y Ohnishi; K Kimura
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1985

Review 2.  Metabolic syndromes with dermatologic manifestations.

Authors:  M Irons; H L Levy
Journal:  Clin Rev Allergy       Date:  1986-02

3.  Prolidase directly binds and activates epidermal growth factor receptor and stimulates downstream signaling.

Authors:  Lu Yang; Yun Li; Yi Ding; Kyoung-Soo Choi; A Latif Kazim; Yuesheng Zhang
Journal:  J Biol Chem       Date:  2012-12-04       Impact factor: 5.157

4.  Biochemical studies on prolidase in sera from control, patients with prolidase deficiency and their mother.

Authors:  T Ohhashi; T Ohno; J Arata; H Kodama
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

5.  In-vitro responses to ascorbate and manganese in fibroblasts from a patient with prolidase deficiency and iminodipeptiduria: cell growth, prolidase activity and collagen metabolism.

Authors:  I Myara; C Charpentier; C Wolfrom; M Gautier; A Lemonnier; M Larregue; A Chamson; J Frey
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

6.  Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases.

Authors:  Francis Rossignol; Marvid S Duarte Moreno; Carlos R Ferreira; Manuel Schiff; Jean-François Benoist; Manfred Boehm; Emmanuelle Bourrat; Aline Cano; Brigitte Chabrol; Claudine Cosson; José Luís Dapena Díaz; Arthur D'Harlingue; David Dimmock; Alexandra F Freeman; María Tallón García; Cheryl Garganta; Tobias Goerge; Sara S Halbach; Jan de Laffolie; Christina T Lam; Ludovic Martin; Esmeralda Martins; Andrea Meinhardt; Isabelle Melki; Amanda K Ombrello; Noémie Pérez; Dulce Quelhas; Anna Scott; Anne M Slavotinek; Ana Rita Soares; Sarah L Stein; Kira Süßmuth; Jenny Thies
Journal:  Genet Med       Date:  2021-05-26       Impact factor: 8.822
  6 in total

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