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GM05520 Fibroblast

Description:

SIALIC ACID STORAGE DISEASE; SIASD

Affected:

Yes

Sex:

Female

Age:

No Data

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Lysosomal Storage Diseases
Class Disorders of Carbohydrate Metabolism
Cell Type Fibroblast
Transformant Untransformed
Race White
Ethnicity YUGOSLAVIAN
Family Member 1
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Yugoslavian; gargoyle-like features; hepatosplenomegaly; severe progressive mental and neurologic involvement; similarly affected brother; markedly elevated free sialic acid in urine and cultured skin fibro; normal acid hydrolases

Characterizations

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Passage Frozen 2
 

Phenotypic Data

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Remarks Yugoslavian; gargoyle-like features; hepatosplenomegaly; severe progressive mental and neurologic involvement; similarly affected brother; markedly elevated free sialic acid in urine and cultured skin fibro; normal acid hydrolases

Publications

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Bardor M, Nguyen DH, Diaz S, Varki A, Mechanism of uptake and incorporation of the non-human sialic acid N-glycolylneuraminic acid into human cells The Journal of biological chemistry280:4228-37 2004
PubMed ID: 15557321
 
Schmid JA, Mach L, Paschke E, Glossl J, Accumulation of sialic acid in endocytic compartments interferes with the formation of mature lysosomes. Impaired proteolytic processing of cathepsin B in fibroblasts of patients with lysosomal sialic acid storage disease. J Biol Chem274:19063-71 1999
PubMed ID: 10383408
 
Hancock LW, Ricketts JP, Hildreth J 4th, Impaired proteolytic processing of lysosomal N-acetyl-beta- hexosaminidase in cultured fibroblasts from patients with infantile generalized N-acetylneuraminic acid storage disease. Biochem Biophys Res Commun152:83-92 1988
PubMed ID: 2965873
 
Tondeur M, Libert J, Vamos E, Van Hoof F, Thomas GH, Strecker G, Infantile form of sialic acid storage disorder: clinical, ultrastructural, and biochemical studies in two siblings. Eur J Pediatr139:142-7 1982
PubMed ID: 7151835

External Links

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dbSNP dbSNP ID: 21797
NCBI GTR 269920 INFANTILE SIALIC ACID STORAGE DISEASE; ISSD
OMIM 269920 INFANTILE SIALIC ACID STORAGE DISEASE; ISSD
Omim Description INFANTILE SIALIC ACID STORAGE DISORDER; ISSD
  N-ACETYLNEURAMINIC ACID STORAGE DISEASE
  NANA STORAGE DISEASE; NSDSIALURIA, FINNISH TYPE, INCLUDED
  SALLA DISEASE; SD, INCLUDED
  SIALIC ACID STORAGE DISEASE; SIASD
  SIALURIA

Culture Protocols

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Passage Frozen 2
Split Ratio 1:5
Temperature 37 C
Percent CO2 5%
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not inactivated
Substrate None specified
Subcultivation Method trypsin-EDTA
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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