Literature DB >> 539707

[Knowledge of Solomon's epidermal nevus syndrome (author's transl)].

O Enjolras, D Guérin, J Hewitt.   

Abstract

Solomon's epidermal nevus syndrome is a questionable entity, because of its clinical heterogeneity. Four cases are presented in this paper, with emphasis on the complex relationship between variable types of epidermal nevi and diverse kinds of associated nervous, ocular and bone abnormalities. Nevertheless, it is of practical interest to know the frequency and the variability of these ectodermal and mesodermal associated defects; whatever the epidermal nevus, a careful examination must be carried out, in search of ocular, nervous, bone and renal signs, and, less frequently, but more often than in other children, these patients seem to be exposed to visceral malignancies.

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Year:  1979        PMID: 539707

Source DB:  PubMed          Journal:  Ann Dermatol Venereol        ISSN: 0151-9638            Impact factor:   0.777


  3 in total

1.  Late occurrence of additional ocular and intracranial pathologies in the linear naevus sebaceous (Feuerstein-Mims) syndrome.

Authors:  J Brihaye; M Brihaye-van Geertruyden; J Retif; A M Mercier
Journal:  Acta Neurochir (Wien)       Date:  1988       Impact factor: 2.216

2.  Computed tomography appearances in the linear sebaceous naevus syndrome.

Authors:  S Levin; R O Robinson; J Aicardi; R D Hoare
Journal:  Neuroradiology       Date:  1984       Impact factor: 2.804

3.  The CHILD syndrome. Congenital hemidysplasia with ichthyosiform erythroderma and limb defects.

Authors:  R Happle; H Koch; W Lenz
Journal:  Eur J Pediatr       Date:  1980-06       Impact factor: 3.183

  3 in total

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