All individuals with variants in gene TPK1

5 entries on 1 page. Showing entries 1 - 5.
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00226664 P76 PubMed: Ortigoza-Escobar 2017 2-generation family, 2 affected, unaffected heterozygous carrier parents - yes China Asian 29m - - - THMD encephalopathy, encephalopathy, hypotonia, spasticity, hypoaesthesia, dysphagia, respiratory failure, seizures; neuroimaging abnormalities: caudate, putamen, globus pallidus, thalamus, brainstem, periqueductal, spinal cord, cerebellum-dentate; 29m-deceased 1 2 Johan den Dunnen
00226665 P77 PubMed: Ortigoza-Escobar 2017 P77 - yes China Asian - - - - THMD encephalopathy, hypotonia, dystonia, spasticity, strabismus, hypoaesthesia, dysphagia; neuroimaging abnormalities: putamen, thalamus, cerebellum-dentate; outcome: spasticity, hypotonia, intellectual disability 1 1 Johan den Dunnen
00226666 P78 PubMed: Ortigoza-Escobar 2017 family, several affected - no Finland white, European 6m - - - THMD hypotonia, liver disease, seizures; neuroimaging abnormalities: putamen, globus pallidus, cerebellum-dentate; 6m-deceased 1 1 Johan den Dunnen
00226667 P79 PubMed: Ortigoza-Escobar 2017 - - yes India - - - - - THMD spasticity; neuroimaging abnormalities: cerebellum-dentate; outcome: spasticity, movement disorder, microcephaly, intellectual disability 1 1 Johan den Dunnen
00269340 - - - F - - - - - - - ? Abnormality of movement (HP:0100022); Dystonia (HP:0001332) 2 1 Andreas Laner
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