Disease #00284 (epilepsy, myoclonic, dystonia, hemiparesis, autonomic signs, lethargy, progressive diffuse cerebral atrophy)

Official abbreviation -
Name epilepsy, myoclonic, dystonia, hemiparesis, autonomic signs, lethargy, progressive diffuse cerebral atrophy
OMIM ID -
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene TBC1D24
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Disease features -
Remarks -
Date created 2013-11-28 15:59:11 +01:00 (CET)
Date last edited 2015-12-08 23:59:30 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00004092 - PubMed: Guven A 2013 - - - - Turkish - - - - epilepsy, myoclonic, dystonia, hemiparesis, autonomic signs, lethargy, progressive diffuse cerebral atrophy - TBC1D24 TBC1D24 1 1 Philippe Campeau
00054868 Pat6 PubMed: van de Warrenburg 2016, Journal: van de Warrenburg 2016 - F - - - - - - - epilepsy, myoclonic, dystonia, hemiparesis, autonomic signs, lethargy, progressive diffuse cerebral atrophy epilepsy and ataxia CACNA1A CACNA1A 1 1 Erik-Jan Kamsteeg
00433663 - - - - - - - - - - - epilepsy, myoclonic, dystonia, hemiparesis, autonomic signs, lethargy, progressive diffuse cerebral atrophy severe intellectual disability, spastic quadriplegia, epilepsy, facial abnormalities - CPA6, TCOF1 2 1 Marketa Wayhelova
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