All individuals with variants in gene MUC4

3 entries on 1 page. Showing entries 1 - 3.
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00056046 - PubMed: Riviere 2012, Journal: Riviere 2012 2-generation family, 3 affected sibs (2F, M), unaffected non-carrier parents/sister; suspected germline mosaicism parent since 3 affected sibs share germline variant not detected in either parent (2 tissues) M no - European >16y - - - MPPH1 mild developmental delay particularly involving speech, later diagnosed with Asperger syndrome; 18m-third ventriculostomy for progressive ventriculomegaly (HP:0002119), no seizures; 12.5y MRI-brain striking megalencephaly (HP:0001355), bilateral perisylvian polymicrogyria (HP:0002126), borderline cerebellar tonsillar ectopia, moderately thick corpus callosum, no vascular malformations, no digital anomalies (no polydactyly (-HP:0010442), no syndactyly (-HP:0001159)) 2 3 Johan den Dunnen
00225725 23749797-FamFC478 PubMed: Nakhro 2013 3-generation family, 3 affected sisters, unaffected heterozygous carrier parents/relatives F no Korea - - - - - CMT see paper; ... 2 3 Johan den Dunnen
00296733 EG76;FamAPatII1 PubMed: Arno 2016 2-generation family, 1 affected, unaffected parents M no - Asia - - - - retinal disease 5y-nyctalopia (HP:0000662), 18y-field constriction (HP:0001133); fundus peripheral retinal atrophy (HP:0200070), vessel attenuation (HP:?), bony spicules (HP:0007737); 20y-ERG photopic responses severely reduced; Goldmann visual fields reduced to 30 degrees with preserved temporal islands, early posterior subcapsular cataract (HP:0007787) 3 1 Johan den Dunnen
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