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
|