All individuals with variants in gene COQ5

4 entries on 1 page. Showing entries 1 - 4.
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00065123 26996948-FamPatV1[EG01] PubMed: Makrythanasis 2016, Journal: Makrythanasis 2016 2-generation family, 2-affected sisters, PatV1[EG01] F yes Egypt - >24y - - Combiantion of valproate and carbamazepine ID seizures (HP:0001250), thin corpus calosum (HP:0002079), asymmetry of the lateral ventricles (HP:?), hypotonia (HP:0001252), hyporeflexia (HP:0001265), joint laxity (HP:0001388), difficulty walking (HP:0002355), dysmorphic features (HP:0001999); profound intellectual disability (HP:0002187); motor delay (HP:0001270); no speech delay (-HP:0000750) 1 2 Jamie Zeegers
00065125 26996948-FamPatV5[EG02] PubMed: Makrythanasis 2016, Journal: Makrythanasis 2016 PatV5[EG02] F yes Egypt - >14y - - Combiantion of valproate and topiramate ID seizures (HP:0001250), thin corpus calosum (HP:0002079), asymmetry of the lateral ventricles (HP:?), hypotonia (HP:0001252), hyporeflexia (HP:0001265), joint laxity (HP:0001388), difficulty walking (HP:0002355), dysmorphic features (HP:0001999); profound intellectual disability (HP:0002187); motor delay (HP:0001270); no speech delay (-HP:0000750) 1 1 Jamie Zeegers
00424946 Fam11 PubMed: Jurkute 2022 2-generation family, 1 affected, unaffected heterozygous carrier mother M - United Kingdom (Great Britain) - - - - - RP 49y-incidental finding during routine check-up, prolonged dark adaptation, peripheral visual field loss; retinitis pigmentosa; hypertension 2 1 Johan den Dunnen
00424951 Fam12 PubMed: Jurkute 2022 2-generation family, 1 affected, unaffected parents F - - - - - - - RP muscle weakness, 14y-vision problems in dark; retinitis pigmentosa, nystagmus; hyposthenia, infantile appearance, hypertelorism, undeveloped fertile function 2 1 Johan den Dunnen
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