Literature DB >> 3643827

Study of elastase-type activity in blister fluids of recessive dystrophic epidermolysis bullosa.

C Francès, G Meimon, S Herson, L Robert.   

Abstract

Recessive dystrophic epidermolysis bullosa (RDEB) is characterized clinically by blister formation due to minor trauma and ultrastructurally by a progressive disappearance of anchoring fibrils at the dermoepidermal junction and of the oxytalan-type fibers which belong to the elastic fiber system. In this study, we determined the elastase-type activity in blister fluid obtained from 8 patients suffering from RDEB as compared to the suction fluid of experimental blisters in a healthy person and to the blister fluid of a patient suffering from epidermolysis bullosa simplex. One patient with dominant dystrophic epidermolysis of the albopapuloid type was also studied. Seven of the eight children with RDEB showed highly elevated values. The eighth child, treated with etretinate, as well as the patient suffering from dominant epidermolysis bullosa had moderately increased values. The determination of elastase-type activity in the blister fluid could therefore be useful to establish the differential diagnosis of recessive dystrophic epidermolysis bullosa.

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Year:  1986        PMID: 3643827

Source DB:  PubMed          Journal:  Clin Physiol Biochem        ISSN: 0252-1164


  1 in total

1.  Exclusion of stromelysin-1, stromelysin-2, interstitial collagenase and fibronectin genes as the mutant loci in a family with recessive epidermolysis bullosa dystrophica and a form of cerebellar ataxia.

Authors:  M Colombi; R Gardella; N Zoppi; L Moro; D Marini; N K Spurr; S Barlati
Journal:  Hum Genet       Date:  1992-07       Impact factor: 4.132

  1 in total

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