All individuals with variants in gene SYNJ1

5 entries on 1 page. Showing entries 1 - 5.
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00001237 - PubMed: Quadri 2013 4-generation family, affected brother/sister - yes Italy Sicily - - - - PD early-onset atypical Parkinsonism, no history of neurological diseases in pre-vious generations 35 2 Marialuisa Quadri
00054710 - - 5-generation family, affected brother/sister, unaffected heterozygous carrier parents - yes India north india - - - - PD rest tremor, bradykinesia, rigidity, postural instability, drooling of saliva, intense dyskinesia and dystonia 1 2 Thelma BK
00292980 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 107 Mohammed Faruq
00324887 Fam21 Journal: Schalk 2020, PubMed: Schalk 2022 2-generation family, 1 affected, unaffected heterozygous carrier parents M - United States - - - - - NDD see paper; ..., birth 40w, weight +0/13SD, OFC -1.3SD; weight -1.7SD, length -2.6SD, OFC -2.07SD; severe intellectual disability/developemental delay; hypotonia; seizures; motor delay; 35m-walk; speech delay; no speech; autistic behaviour; stereotypies; hyperactivity; feeding difficulties; sleeping disturbance; almond eyes; thin upper lip; epicanthus 1 1 Johan den Dunnen
00405036 107758 - - M yes Turkey - - - - - EIEE53 Global developmental delay, Seizure, Generalized-onset seizure, Gait disturbance, Gait ataxia, Febrile seizure (within the age range of 3 months to 6 years), Seizure precipitated by febrile infection, EEG abnormality, Abnormal cerebral white matter morphology, Abnormal cerebral morphology, Abnormality of visual evoked potentials, Abnormal timing of flash visual evoked potentials, Abnormality of metabolism/homeostasis, Hypotonia, Infantile axial hypotonia, Recurrent fever, Fever, Oral motor hypotonia, Restlessness, Short attention span 1 1 Andreas Laner
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