All individuals with variants in gene CARS2

6 entries on 1 page. Showing entries 1 - 6.
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00263964 PKRD320 III:4 PubMed: Biswas 2018 3-generation family, 3 affected M yes Pakistan - - - - - retinal degeneration, retinal disease inherited retinal degeneration (HP:0000546), retinal dystrophy (HP:0000556) 1 3 Jasmine Chen
00269908 - - - ? - - - - - - - ? Developmental regression (HP:0002376); Mental deterioration (HP:0001268); Progressive microcephaly (HP:0000253); Seizures (HP:0001250); Progressive visual loss (HP:0000529); Progressive hearing impairment (HP:0001730) 1 1 IMGAG
00290840 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 90 Mohammed Faruq
00290841 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00305912 Pat4 PubMed: Marcogliese 2018 2-generation family, 1 affected, unaffected parents F - - - - - - - NDD, VMD no dysmorphisms; motor regression present (age onset unknown); 12y-single words; unsteady gait, clumsy, 12y-mostly wheelchair-bound; 12y-loss of fine motor skills; excessive drooling; 12y-lost continence; 15y-lower extremity dystonia; bilateral ptosis, macular degeneration; 12y-poor balance; Bracken Basics Concepts III Receptive and School Readiness Composite, Conner’s Parent Rating Scale, 6y-Child Behavior Checklist intellectual functioning at approximately 1-3 year level; 13y-epilepsy, spells that consist of falling that last about 1 min; EEG 6.5y-no electrographic or electroclinical sz, but photic stim produced photoconvulsive response, 13y-moderately abnormal - recorded photo myoclonic sz during intermittent photic stim, generalized interictal epileptiform features, sleep architecture was additionally somewhat disrupted with high-voltage rhythmic delta; MRI brain 6y-normal, 13y-normal, 15y-thin corpus callosum but overall within normal limits, MRI brain 13y-spine normal, 15y-spine normal 1 1 Johan den Dunnen
00403884 TF067 PubMed: Froukh 2020 analysis 103 families with neurodevelopmental disorders; family, 2 affected sibs - - Jordan - - - - - NDD severe developmental regression 1 2 Johan den Dunnen
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