Literature DB >> 3922107

An autopsy case of prolidase deficiency.

M Sekiya, Y Ohnishi, K Kimura.   

Abstract

A 25-year-old female who suffered from longstanding incurable leg ulcers was found to have prolidase deficiency with iminodipeptiduria. On ultrastructural studies of autopsy specimens, the lamina densa of the epidermal basement membrane was found to show irregular splitting and the basement membranes of the dermal blood vessels were lamellated with interruptions. Lamellar changes and splitting of the basement membranes of the renal tubules, interstitial blood vessels and glomerular capillaries also occurred. These morphological abnormalities seem to be one of causes of the clinical symptomatology.

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Year:  1985        PMID： 3922107     DOI： 10.1007/bf00710562

Source DB:  PubMed          Journal:  Virchows Arch A Pathol Anat Histopathol        ISSN： 0174-7398


  18 in total

1.  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

2.  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

3.  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

4.  Secretion of collagen by embryonic neuroepithelium at the time of spinal cord--somite interaction.

Authors:  A M Cohen; E D Hay
Journal:  Dev Biol       Date:  1971-12       Impact factor: 3.582

5.  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

6.  Potassium permanganate reaction in amyloidosis. A histologic method to assist in differentiating forms of this disease.

Authors:  J R Wright; E Calkins; R L Humphrey
Journal:  Lab Invest       Date:  1977-03       Impact factor: 5.662

7.  Prolidase deficiency.

Authors:  P S Pedersen; E Christensen; N J Brandt
Journal:  Acta Paediatr Scand       Date:  1983-09

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

Authors:  C Charpentier; K Dagbovie; A Lemonnier; M Larregue; R A Johnstone
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

9.  Autosomal recessive prolidase deficiency. Three patients with recalcitrant ulcers.

Authors:  A Ogata; S Tanaka; T Tomoda; E Murayama; F Endo; I Kikuchi
Journal:  Arch Dermatol       Date:  1981-11

10.  Studies on prolidase deficiency with a possible defect in collagen metabolism.

Authors:  M Isemura; T Hanyu; T Ono; R Igarashi; Y Sato; F Gejyo; R Nakazawa; T Miyakawa; T Takagi; Y Kuboki; S Sasaki
Journal:  Tohoku J Exp Med       Date:  1981-05       Impact factor: 1.848
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  3 in total

1.  Prolidase deficiency associated with systemic lupus erythematosus (SLE): single site experience and literature review.

Authors:  Yonatan Butbul Aviel; Hana Mandel; Emily Avitan Hersh; Reuven Bergman; Orly Eshach Adiv; Anthony Luder; Riva Brik
Journal:  Pediatr Rheumatol Online J       Date:  2012-06-22       Impact factor: 3.054

2.  The effect of estrogen on prolidase-dependent regulation of HIF-1α expression in breast cancer cells.

Authors:  Arkadiusz Surazynski; Wojciech Miltyk; Izabela Prokop; Jerzy Palka
Journal:  Mol Cell Biochem       Date:  2013-04-03       Impact factor: 3.396

3.  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
  3 in total

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