Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4-5
pubmed:dateCreated
1992-7-9
pubmed:abstractText
Pseudodeficiency is defined as the in vitro measurement of low activity (usually under 15% of the normal mean for controls) of an enzyme in a healthy person. They may be hard to distinguish from presymptomatic people who will present with adult-onset clinical disease. The finding of healthy people with low arylsulfatase A and galactocerebrosidase activities is well documented. This confuses the laboratory doing testing and the clinician providing the sample. Therefore confirmation of a diagnosis of metachromatic leukodystrophy and Krabbe disease, as well as accurate identification of carriers, requires additional testing including 14C-sulfatide loading in cultured skin fibroblasts, examination of urine for excretion of undegraded lipids, examination of enzyme levels in additional family members including grandparents, and molecular analysis of DNA samples for known mutations.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0378-5866
pubmed:author
pubmed:issnType
Print
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
216-21
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:1687777-Adult, pubmed-meshheading:1687777-Cells, Cultured, pubmed-meshheading:1687777-Cerebroside-Sulfatase, pubmed-meshheading:1687777-Child, pubmed-meshheading:1687777-Clinical Enzyme Tests, pubmed-meshheading:1687777-DNA, pubmed-meshheading:1687777-Diagnosis, Differential, pubmed-meshheading:1687777-False Negative Reactions, pubmed-meshheading:1687777-Female, pubmed-meshheading:1687777-Fetal Diseases, pubmed-meshheading:1687777-Fibroblasts, pubmed-meshheading:1687777-Galactosylceramidase, pubmed-meshheading:1687777-Gene Frequency, pubmed-meshheading:1687777-Genetic Complementation Test, pubmed-meshheading:1687777-Heterozygote Detection, pubmed-meshheading:1687777-Humans, pubmed-meshheading:1687777-Leukocytes, pubmed-meshheading:1687777-Leukodystrophy, Globoid Cell, pubmed-meshheading:1687777-Leukodystrophy, Metachromatic, pubmed-meshheading:1687777-Male, pubmed-meshheading:1687777-Middle Aged, pubmed-meshheading:1687777-Polymerase Chain Reaction, pubmed-meshheading:1687777-Pregnancy, pubmed-meshheading:1687777-Prenatal Diagnosis
pubmed:year
1991
pubmed:articleTitle
Pseudodeficiencies of arylsulfatase A and galactocerebrosidase activities.
pubmed:affiliation
Department of Medicine (Medical Genetics), Jefferson Medical College, Philadelphia, Pa.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't