Literature DB >> 7686542

[Lipoid proteinosis in 2 sisters].

G Oezarmağan1, C Baykal, E O Gürsoy, S Yilmazer, N Büyükbabani, O Coban.   

Abstract

Lipoid proteinosis was diagnosed in two daughters of a consanguinous marriage on the basis of genetic, clinical, light microscopic and ultrastructural findings. Hyaline material accumulation, thickening of the basal laminae and the resulting typical onion skin phenomenon were observed. In addition to the pathognomonic cutaneous mucosal findings, unusual manifestations such as persistence of deciduous teeth (in one case), oligodontia and intracerebral calcifications were observed. In one patient, the intracerebral calcifications caused epileptic seizures.

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Year:  1993        PMID: 7686542

Source DB:  PubMed          Journal:  Hautarzt        ISSN: 0017-8470            Impact factor:   0.751


  1 in total

1.  Unknown syndrome: peculiar face, severe hypodontia of permanent teeth, and precocious choroid calcifications.

Authors:  R Pallotta; P Fusilli
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318

  1 in total

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