Linked Life Data

4080094

Source:http://linkedlifedata.com/resource/pubmed/id/4080094

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1986-1-31
pubmed:abstractText
Non-ketotic hyperglycinemia (NKH) has been differentiated as an autosomal recessive hereditary form of the hyperglycinemias with a defect in the glycine-cleavage system causing accumulation of glycine in all body fluids. A more severe neonatal form with early onset has been described and, though not curable, a fast and correct diagnosis for clinical management, parental information and genetic counselling is important. The clinical picture and diagnostic chemical analyses in two cases of the more severe neonatal form of NKH are reported.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0174-304X
pubmed:author
pubmed:issnType
Print
pubmed:volume
16
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
191-3
pubmed:dateRevised
2008-1-16
pubmed:meshHeading
pubmed:year
1985
pubmed:articleTitle
Neonatal non-ketotic hyperglycinemia (NKH). Diagnoses and management in two cases.
pubmed:publicationType
Journal Article, Case Reports