Literature DB >> 402253

Fucosidosis.

E B Smith, J L Graham, J A Ledman, R D Snyder.   

Abstract

Disseminated angiokeratomas can be seen in patients with an inherited deficiency of alpha-l-fucosidase as well as in patients with classic Fabry's disease. Patients with deficiency of this lysosomal enzyme, or fucosidosis, have spasticity, mental retardation, and retardation of growth in addition to angiokeratomas. We herein report three new cases of this rare syndrome.

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Year:  1977        PMID: 402253

Source DB:  PubMed          Journal:  Cutis        ISSN: 0011-4162


  3 in total

Review 1.  Metabolic syndromes with dermatologic manifestations.

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

2.  Fucosidosis: ultrastructural study of the eye in an adult.

Authors:  M Hoshino; T P O'Brien; J M McDonnell; Z C de la Cruz; W R Green
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1989       Impact factor: 3.117

3.  Angiokeratoma corporis diffusum with features of a mucopolysaccharidosis.

Authors:  D I McCallum; R F Macadam; A W Johnston
Journal:  J Med Genet       Date:  1980-02       Impact factor: 6.318

  3 in total

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