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Genomic newborn screening: BabyScreen+ v0.1896 LIAS Zornitza Stark Marked gene: LIAS as ready
Genomic newborn screening: BabyScreen+ v0.1896 LIAS Zornitza Stark Gene: lias has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.1896 LIAS Zornitza Stark Publications for gene: LIAS were set to PMID: 24334290, 24777537,
Genomic newborn screening: BabyScreen+ v0.1895 LIAS Zornitza Stark Source Expert list was removed from LIAS.
Source Expert Review was added to LIAS.
Rating Changed from No List (delete) to Red List (low evidence)
Genomic newborn screening: BabyScreen+ v0.1894 LIAS Zornitza Stark All sources for gene: LIAS were removed
Genomic newborn screening: BabyScreen+ v0.1893 LIAS Zornitza Stark All sources for gene: LIAS were removed
Genomic newborn screening: BabyScreen+ v0.1892 LIAS Zornitza Stark Classified gene: LIAS as Red List (low evidence)
Genomic newborn screening: BabyScreen+ v0.1892 LIAS Zornitza Stark Gene: lias has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.1872 LIAS Lilian Downie gene: LIAS was added
gene: LIAS was added to gNBS. Sources: Expert list
Mode of inheritance for gene: LIAS was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: LIAS were set to PMID: 24334290, 24777537,
Phenotypes for gene: LIAS were set to Hyperglycinemia, lactic acidosis, and seizures MIM#614462
Review for gene: LIAS was set to RED
Added comment: pyruvate dehydrogenase lipoic acid synthetase deficiency (PDHLD)
increased serum glycine and lactate in the first days of life, hypotonia, seizures, early death
No treatment
Sources: Expert list