Disease #03661 (BSVD2;POREN2 (brain small vessel disease, type 2 (BSVD2);porencephaly type 2 (POREN2)), OMIM:614483)

Official abbreviation BSVD2;POREN2
Name brain small vessel disease, type 2 (BSVD2);porencephaly type 2 (POREN2)
OMIM ID 614483
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene COL4A2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-04-21 11:49:40 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00296453 - - - - - - - - - - - BSVD2;POREN2 - COL4A1, COL4A2 COL4A2 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00363527 177212 - - M ? Germany - - - - - BSVD2;POREN2 Dystonic movement disorder, severe generalised dystonia, scoliosis, epilepsy (myoclonic), porencephaly, cognition less affected than motor function, no speech, no voluntary motor function, sister with mild porencephaly COL4A2 COL4A2 1 1 Andreas Laner
00448541 288388 - - F no Germany - - - - - BSVD2;POREN2 Cerebral palsy, Hemiparesis, Periventricular leukomalacia, Ventriculomegaly, Esodeviation, Delayed speech and language development, Delayed gross motor development, EEG with focal sharp waves, Abnormality of refraction, Symptomatic seizures COL4A2 COL4A2 1 1 Andreas Laner
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