Disease #00061 (CLN8 (lipofuscinosis, ceroid, neuronal, type 8 (CLN-8)), OMIM:600143)

Official abbreviation CLN8
Name lipofuscinosis, ceroid, neuronal, type 8 (CLN-8)
OMIM ID 600143
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene CLN8
Associated tissues -
Disease features -
Remarks -
Date created 2012-10-11 12:20:05 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00307876 ? - - F ? Oman - - - - - CLN8 Febrile seizures, Developmental regression, Brain atrophy CLN8 CLN8 1 1 Corina-Marcela Rus
00307896 ? - - F no Ukraine - - - - - CLN8 Ptosis, Dementia, Seizures, Ataxia, Hemiparesis, Gait disturbance, Encephalopathy, Generalized-onset seizure, Developmental regression, Aphasia, Leukodystrophy, Abnormal myelination, Neurodevelopmental abnormality CLN8 CLN8 1 1 Corina-Marcela Rus
00380774 ? PubMed: Nair 2018 - ? - Lebanon - - - - - CLN8 DD; ID; seizures; regression; cerebellar atrophy (Neurological) - CLN8 1 1 LOVD
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