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This section gives an overview of the disease, and where available shows the following:
More information can be found in the help pages.
✖Disease ID: | 144 | |
Name: | Bilateral frontoparietal polymicrogyria | |
Associated with: | 1 target |
Database Links |
OMIM:
606854 Orphanet: ORPHA101070 |
Click on the target name to link to its detailed view page
Where available, information is display on the role of the target in the disease; drugs which target the disease and their therapeutic use and side-effects.
If there is mutation data curated in GtoPdb this is indicated, with a link back to the appropriate section on the target detailed view page
Immuno ligand interactions - If available, a table of immuno-relevant ligands is shown. These ligands have been curated as having an association to the disease and possess interaction data with the target in GtoPdb. The approval status of the ligand is shown, along with curator comments and an indication of whether the target is considered the primary target of the ligand.
More information can be found in the help pages.
✖ADGRG1 | |
Comments: | A human brain cortical malformation called bilateral frontoparietal polymicrogyria cortex is associated with one of eleven different mutations of ADGRG1. |
References: | 1-6 |
Mutations: | ADGRG1 is associated with 14 mutation. Click here for details ![]() |
Click ligand name to view ligand summary page
Click the arrow in the final column to expand comments
More information can be found in the help pages.
✖No ligand related data available for Bilateral frontoparietal polymicrogyria
1. Bahi-Buisson N, Poirier K, Boddaert N, Fallet-Bianco C, Specchio N, Bertini E, Caglayan O, Lascelles K, Elie C, Rambaud J et al.. (2010) GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex. Brain, 133 (11): 3194-209. [PMID:20929962]
2. Luo R, Yang HM, Jin Z, Halley DJ, Chang BS, MacPherson L, Brueton L, Piao X. (2011) A novel GPR56 mutation causes bilateral frontoparietal polymicrogyria. Pediatr Neurol, 45 (1): 49-53. [PMID:21723461]
3. Parrini E, Ferrari AR, Dorn T, Walsh CA, Guerrini R. (2009) Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutations. Epilepsia, 50 (6): 1344-53. [PMID:19016831]
4. Piao X, Chang BS, Bodell A, Woods K, Benzeev B, Topcu M, Guerrini R, Goldberg-Stern H, Sztriha L, Dobyns WB et al.. (2005) Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes. Ann Neurol, 58 (5): 680-7. [PMID:16240336]
5. Piao X, Hill RS, Bodell A, Chang BS, Basel-Vanagaite L, Straussberg R, Dobyns WB, Qasrawi B, Winter RM, Innes AM et al.. (2004) G protein-coupled receptor-dependent development of human frontal cortex. Science, 303 (5666): 2033-6. [PMID:15044805]
6. Quattrocchi CC, Zanni G, Napolitano A, Longo D, Cordelli DM, Barresi S, Randisi F, Valente EM, Verdolotti T, Genovese E et al.. (2013) Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotype. Neurogenetics, 14 (1): 77-83. [PMID:23274687]