All individuals with variants in gene SPRTN

5 entries on 1 page. Showing entries 1 - 5.
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00038712 - PubMed: Lessel 2014, Journal: Lessel 2014 - M yes Morocco - 17y - - - ? see papaer; early onset hepatocellular carcinoma, genomic instability, progeroid features, ... 1 1 Davor Lessel
00038736 - PubMed: Lessel 2014, Journal: Lessel 2014 2-generation family, 2 affected brothers, unaffected heterozygous carrier parents M no Australia European 18y - - - ? see paper; early onset hepatocellular carcinoma, genomic instability, progeroid features, ... 2 2 Johan den Dunnen
00038737 - PubMed: Lessel 2014, Journal: Lessel 2014 2-generation family, 2 affected brothers, unaffected heterozygous carrier parents M no Australia European - - - - ? see paper; early onset hepatocellular carcinoma, genomic instability, progeroid features, ... 2 1 Johan den Dunnen
00443879 FamEPatIII2 PubMed: Chatron 2020 3-generation family, 2 affected brothesr, unaffected heterozygous parents/relatives M yes Turkey - - - - - DEE see paper; ..., 1m-epileptic spasms; 2m-seizure-free; EEG at onset hypsarrhythmic; axial hypotonia, spasticity; profound intellectual disability; pes equinovarus; no omphalocele; cleft palate; joint contractures; dysmorphic facial features; MRI brain 50d-normal, CT 2m-atlanto-axial anomaly, minimal hydrocephalus 1 2 Johan den Dunnen
00443880 FamEPatIII1 PubMed: Chatron 2020 brother M yes Turkey - 9d - - - DEE see paper; ..., 9d-deceased; 1d-myoclonic seizure; pes equinovarus; no omphalocele; cleft palate; no joint contractures; no dysmorphic facial features; cranial ultrasound germinal matrix haemorrhage 1 1 Johan den Dunnen
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