Disease #05083 (BVVLS (Brown-Vialetto-Van Laere syndrome (BVVLS)))

Official abbreviation BVVLS
Name Brown-Vialetto-Van Laere syndrome (BVVLS)
OMIM ID -
Inheritance -
Individuals reported having this disease 8
Phenotype entries for this disease 4
Associated with 2 genes SLC52A2, SLC52A3
Associated tissues -
Disease features -
Remarks -
Date created 2015-10-12 14:53:07 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00386512 family PubMed: Megarbane 2000, PubMed: Foley 2014 6-generation family, 4 affected (F, 3M), unaffected heterozygous carrier parents/relatives F;M yes Lebanon Shiite;Muslim - - - - BVVLS see paper; ... SLC52A2 SLC52A2 1 1 Johan den Dunnen
00386513 family PubMed: Johnson 2012 6-generation family, 4 affected (F, 3M), unaffected heterozygous carrier parents/relatives F;M yes Lebanon - - - - - BVVLS see paper; ..., progressive sensorineural deafness, childhood amyotrophic lateral sclerosis SLC52A2 MAPK15, SLC52A2 2 1 Johan den Dunnen
00386514 FamD;PatE1 PubMed: Johnson 2012, PubMed: Foley 2014 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Scotland - - - - - BVVLS - SLC52A2 SLC52A2 1 1 Johan den Dunnen
00386515 patient PubMed: Johnson 2012 - - - - - - - - - BVVLS - SLC52A3 SLC52A3 2 1 Johan den Dunnen
00386516 patient PubMed: Johnson 2012 - - - - - - - - - BVVLS - SLC52A3 SLC52A3 1 1 Johan den Dunnen
00386517 patient PubMed: Haack 2012 2-generation family, 1 affected, unaffected heterozygous carrier parents F no Germany - - - - - BVVLS - SLC52A2 SLC52A2 2 1 Johan den Dunnen
00386536 FamDZ PubMed: Johnson 2010 4-generation family, 3 affected (3F), unaffected heterozygous carrier parents/relatives F yes Turkey - - - - - BVVLS - SLC52A3 SLC52A3 1 1 Johan den Dunnen
00472908 Fam9648Pat5 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history F no Iran - - - - - BVVLS onset 14y with GI problem including dysphagia, nausea and weight loss; Sensorineural hearing loss; Hand tremor; Atrophy of thenar and hypothenar; Mild generalized muscle weakness; EMG-NCV: motor neuron disease. - SLC52A2 2 1 Johan den Dunnen
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