All individuals with variants in gene VPS4A

14 entries on 1 page. Showing entries 1 - 14.
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00302775 985.382 PubMed: Hamdan 2015 - M - Canada - - - - - ID severe intellectual disability; no speech; not walking; no epilepsy; no autistic features; acquired microcephaly; no macrocephaly; MRI brain atrophy, ventriculomegaly, decreased white matter and thin corpus callosum; central hypotonia, spasticity; no congenitial malformations; no cardiac malformations; no urogenitory abnormalities 1 1 Johan den Dunnen
00320213 Pat1 PubMed: Seu 2020, Journal: Seu 2020 - F - United States European;Hispanic-American - - - - NDD increased irritability when anemia worsens; transfusion every 4–6 weeks; severe global developmental delay, microcephaly, microgyria, dystonia (axial hypotonia with appendicular hypertonia), suspected Leber congenital amaurosis and/or cortical blindness, failure to thrive, frequent urinary tract infections 1 1 Johan den Dunnen
00320214 Pat2 PubMed: Seu 2020, Journal: Seu 2020 - M - United States European;Hispanic-American - - - - NDD transfusion every 4–10 weeks; severe global developmental delay, seizure disorder, microcephaly, microgyria, dystonia (axial hypotonia with appendicular hypertonia), congenital bilateral cataracts, failure to thrive, chronic kidney disease (stage II-III) 1 1 Johan den Dunnen
00320215 Pat3 PubMed: Seu 2020, Journal: Seu 2020 - F - - Arab - - - - NDD transfusion occasionally (every 2-6m); global developmental delay, macrocephaly, dystonia (axial hypotonia with appendicular hypertonia), delayed myelination, esotropia, frequent urinary tract infections 1 1 Johan den Dunnen
00320217 Pat1 PubMed: Rodger 2020, Journal: Rodger 2020 2-generation family, 1 affected, unaffected non-carrier parents F - United Kingdom (Great Britain) white - - - - NDD see paper; ..., severe intellectual disability 1 1 Johan den Dunnen
00320218 Pat2 PubMed: Rodger 2020, Journal: Rodger 2020 2-generation family, 1 affected, unaffected non-carrier parents M - Italy white 29y - - - NDD see paper; ..., severe intellectual disability 1 1 Johan den Dunnen
00320219 Pat3 PubMed: Rodger 2020, Journal: Rodger 2020 2-generation family, 1 affected, unaffected non-carrier parents M - United Kingdom (Great Britain) white 26m - - - NDD see paper; ..., severe intellectual disability 1 1 Johan den Dunnen
00320220 Pat4 PubMed: Rodger 2020, Journal: Rodger 2020 2-generation family, 1 affected, unaffected non-carrier parents F - - white - - - - NDD see paper; ..., severe intellectual disability 1 1 Johan den Dunnen
00320221 Pat5 PubMed: Rodger 2020, Journal: Rodger 2020 2-generation family, 1 affected, unaffected non-carrier parents F - United States white - - - - NDD see paper; ..., severe intellectual disability 1 1 Johan den Dunnen
00320222 Pat6 PubMed: Rodger 2020, Journal: Rodger 2020 2-generation family, 1 affected, unaffected non-carrier parents M - United Kingdom (Great Britain) white - - - - NDD see paper; ..., severe intellectual disability 1 1 Johan den Dunnen
00320223 Fam PubMed: Rodger 2020, Journal: Rodger 2020 - - - United States - - - - - ? - 1 1 Johan den Dunnen
00320224 Fam PubMed: Rodger 2020, Journal: Rodger 2020 - - - United States - - - - - ? - 1 1 Johan den Dunnen
00320225 Fam PubMed: Rodger 2020, Journal: Rodger 2020 - - - United States - - - - - ? - 1 1 Johan den Dunnen
00320226 Fam PubMed: Rodger 2020, Journal: Rodger 2020 - - - United States - - - - - ? - 1 1 Johan den Dunnen
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