Hydrocephalus
Gene: PLG
As discussed with the GMS Neurology Specialist Test Group webex call 11th July 2019: The Specialist Test Group all agreed that there is enough evidence to rate this gene GreenCreated: 29 Jul 2019, 2:49 p.m. | Last Modified: 29 Jul 2019, 2:49 p.m.
Panel Version: 1.34
Three unrelated cases reported to date; sufficient for causation. Largest review showed 4/50 cases with obstructive hydrocephalus in addition to ligneous conjuncitivitis.Created: 9 May 2017, 1:23 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Plasminogen deficiency, type I
Publications
Phenotypes for gene: PLG were changed from Plasminogen deficiency, type I, OMIM:217090 to Plasminogen deficiency, type I, OMIM:217090; Dysplasminogenemia, OMIM:217090
Phenotypes for gene: PLG were changed from Plasminogen deficiency, type I to Plasminogen deficiency, type I, OMIM:217090
Source NHS GMS was added to PLG.
31.05.2017 - panel revised after internal curation and clinical review.
This gene has been classified as Green List (High Evidence).
PLG was added to Hydrocephaluspanel. Source: Expert Review Green
PLG was added to Hydrocephaluspanel. Sources: Literature
PLG was created by helen.brittain