Presentation of mucopolysaccharidosis VII (beta-glucuronidase deficiency) in infancy.
Open Access
- 1 June 1981
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 18 (3) , 237-239
- https://doi.org/10.1136/jmg.18.3.237
Abstract
A child is presented with mucopolysaccharidosis VII (beta-glucuronidase deficiency), bringing to six the number of reported patients with the infantile onset form of this disorder. This patient exhibited the following features, previously unrecognised as part of this syndrome: presentation in the neonatal period, progressive joint contractures, and hydrocephalus. This child's course and data from published reports indicate that mucopolysaccharidosis VII, unlike the other known mucopolysaccharidoses, is clinically recognisable in the newborn period and is most likely to be associated with moderate mental deficiency which does not progress over time.This publication has 6 references indexed in Scilit:
- Beta-glucuronidase deficiency in a girl with unusual clinical featuresEuropean Journal of Pediatrics, 1977
- Variation in the phenotypic expression of β-glucuronidase deficiencyThe Journal of Pediatrics, 1975
- Mucopolysaccharidosis VII: ?-Glucuronidase deficiencyHuman Genetics, 1974
- Beta glucuronidase deficiency: Report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosisThe Journal of Pediatrics, 1973
- I-Cell Disease: Biochemical StudiesPediatric Research, 1972