Literature DB >> 6494932

Mucolipidosis I. Roentgenographic follow-up.

C R Staalman, H D Bakker.   

Abstract

A patient with mucolipidosis I (ML I) is presented. The roentgenographic findings in the skull, hands, ribs, vertebral column, pelvis, and tubular bones are described. Special emphasis is laid on the evaluation of the skeletal alterations during a 13-years follow-up. The similarities to and the differences from the so-called dysostosis multiplex (DM) are outlined. Some peculiarities which may be specific to ML I are discussed. Attention is given to an exceptional feature in our case of this very rare condition, namely, the marked thickening which developed on the frontal portions of the base of the skull, including the sellar region.

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Year:  1984        PMID: 6494932     DOI: 10.1007/bf00361081

Source DB:  PubMed          Journal:  Skeletal Radiol        ISSN: 0364-2348            Impact factor:   2.199


  14 in total

Review 1.  Sialidosis: a review of human neuraminidase deficiency.

Authors:  J A Lowden; J S O'Brien
Journal:  Am J Hum Genet       Date:  1979-01       Impact factor: 11.025

2.  The genetic mucolipidoses. Diagnosis and differential diagnosis.

Authors:  J W Spranger; H R Wiedemann
Journal:  Humangenetik       Date:  1970

3.  Mucolipidosis I: increased sialic acid content and deficiency of an alpha-N-acetylneuraminidase in cultured fibroblasts.

Authors:  M Cantz; J Gehler; J Spranger
Journal:  Biochem Biophys Res Commun       Date:  1977-01-24       Impact factor: 3.575

4.  Isolated acid neuraminidase deficiency: a distinct lysosomal storage disease.

Authors:  T E Kelly; G Graetz
Journal:  Am J Med Genet       Date:  1977

5.  Neuraminidase deficiency in the cherry red spot-myoclonus syndrome.

Authors:  J S O'Brien
Journal:  Biochem Biophys Res Commun       Date:  1977-12-21       Impact factor: 3.575

6.  Sialidase (alpha-n-acetyl neuraminidase) deficiency: the enzyme defect in an adult with macular cherry-red spots and myoclonus without dementia.

Authors:  G H Thomas; R E Tipton; L T Ch'ien; L W Reynolds; C S Miller
Journal:  Clin Genet       Date:  1978-04       Impact factor: 4.438

7.  Mucolipidosis I (acid neuraminidase deficiency). Three cases and delineation of the variability of the phenotype.

Authors:  T E Kelly; L Bartoshesky; D J Harris; R G McCauley; M Feingold; G Schott
Journal:  Am J Dis Child       Date:  1981-08

8.  Two genetically different MU-NANA neuraminidases in human leucocytes.

Authors:  F W Verheijen; H C Janse; O P van Diggelen; H D Bakker; M C Loonen; P Durand; H Galjaard
Journal:  Biochem Biophys Res Commun       Date:  1983-12-16       Impact factor: 3.575

9.  Mucolipidosis I--a sialidosis.

Authors:  J Sphranger; J Gehler; M Cantz
Journal:  Am J Med Genet       Date:  1977

10.  Sialidosis (mucolipidosis I).

Authors:  P Durand; R Gatti; S Cavalieri; C Borrone; M Tondeur; J C Michalski; G Strecker
Journal:  Helv Paediatr Acta       Date:  1977-11
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