All individuals with variants in gene CARD8

2 entries on 1 page. Showing entries 1 - 2.
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00019841 - PubMed: Gilissen 2014 - F ? - - - - - - ID ID from infancy, regression at adult age; shows parkinsonism and dystonia 1 1 Marianne Vos (LOVD-team)
00305534 Pat1;Individual 20 PubMed: Kruszka 2019, PubMed: Vissers 2020 2-generation family, 1 affected, unaffected non-carrier parents M - United States - - - - - NDD see paper; ..., birth 35w, OFC; Microcephaly; developmental delay; motor delay; speech delay; no epilepsy, Isolated seizure associated with fentanyl administration, normal EEG; hypotonia; facial abnormalities; Pancreatic exocrine deficiency treated with enzyme therapy; Pancreatic insufficiency: neonatal diabetes mellitus requiring insulin therapy; Bilateral conductive and sensorineural hearing loss (R>L), CT scan showed ossicle anomalies; no vision abnormalities; Intrauterine growth restriction; MRI-brain semilobar 1 1 Johan den Dunnen
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