Literature DB >> 1839643

[Mucopolysaccharidosis IS: Scheie's syndrome. A report of 2 brothers].

G Bonora1, D Frattini, M Nedbal, C Massironi, L Perletti.   

Abstract

We describe two brothers affected by MPS type IS (Scheie syndrome). Mucopolysaccharidosis type I consists of three clinical entities of varying severity, all due to alfalevo-iduronidase enzyme deficiency. The MPS IS in characterized by joint stiffness, aortic valve disease and corneal clouding. The intellect is normal. All these findings are present on our brothers; furthermore retinal degeneration also occurred. It could give in the future attendant deterioration of vision.

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Year:  1991        PMID: 1839643

Source DB:  PubMed          Journal:  Pediatr Med Chir        ISSN: 0391-5387


  1 in total

1.  Stereological and morphometric analysis of dermal fibroblasts before and after bone marrow transplantation in a case of mucopolysaccharidosis I Scheie phenotype.

Authors:  M Costa; J García Valero; C Navarro
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

  1 in total

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