Literature DB >> 3809113

Prenatal diagnosis and confirmation of infantile sialic acid storage disease.

E Vamos, J Libert, N Elkhazen, E Jauniaux, J Hustin, P Wilkin, J Baumkötter, K Mendla, M Cantz, G Strecker.   

Abstract

Amniocentesis was performed in a pregnancy at risk for infantile sialic acid storage disease. Greatly elevated levels of free sialic acid were found in cell-free amniotic fluid as well as in cultured amniotic cells from the fetus at risk. After incubation of the cultured amniocytes with fetuin labelled in its sialic acid moiety, pulse and chase experiments respectively showed accumulation and impaired release of TCA-soluble radioactive material in the amniotic cells at risk. These data thus clearly indicated that the fetus was affected. After pregnancy termination, ultrastructural studies of fetal organs and placenta showed a generalized storage picture characterized by clear membrane-bound inclusions. The diagnosis was further confirmed by the finding of greatly increased amounts of free sialic acid in fetal organs and cultured fibroblasts.

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Year:  1986        PMID: 3809113     DOI: 10.1002/pd.1970060607

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  9 in total

1.  Infantile sialic acid storage disease in two siblings.

Authors:  A Cooper; I B Sardharwalla; M Thornley; K P Ward
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

2.  Prenatal diagnosis of infantile sialic acid storage disease in a twin pregnancy.

Authors:  B D Lake; E P Young; K Nicolaides
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

Review 3.  Disorders of glycoprotein degradation.

Authors:  M Cantz; B Ulrich-Bott
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

4.  The genetic locus for free sialic acid storage disease maps to the long arm of chromosome 6.

Authors:  L Haataja; J Schleutker; A P Laine; M Renlund; M L Savontaus; C Dib; J Weissenbach; L Peltonen; P Aula
Journal:  Am J Hum Genet       Date:  1994-06       Impact factor: 11.025

5.  Haplotype analysis in prenatal diagnosis and carrier identification of Salla disease.

Authors:  J Schleutker; P Sistonen; P Aula
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

6.  Lysosomal free sialic acid storage disorders with different phenotypic presentations--infantile-form sialic acid storage disease and Salla disease--represent allelic disorders on 6q14-15.

Authors:  J Schleutker; P Leppänen; J E Månsson; A Erikson; J Weissenbach; L Peltonen; P Aula
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

7.  Defective lysosomal release of glycoprotein-derived sialic acid in fibroblasts from patients with sialic acid storage disease.

Authors:  K Mendla; J Baumkötter; C Rosenau; B Ulrich-Bott; M Cantz
Journal:  Biochem J       Date:  1988-02-15       Impact factor: 3.857

8.  Salla disease variant in a Dutch patient. Potential value of polymorphonuclear leucocytes for heterozygote detection.

Authors:  G M Mancini; P Hu; F W Verheijen; O P van Diggelen; H C Janse; W J Kleijer; F A Beemer; F G Jennekens
Journal:  Eur J Pediatr       Date:  1992-08       Impact factor: 3.183

9.  Biochemical characterization of patients and prenatal diagnosis of sialic acid storage disease for three families.

Authors:  P R Clements; J A Taylor; J J Hopwood
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

  9 in total

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