All individuals with variants in gene SLC9A1

4 entries on 1 page. Showing entries 1 - 4.
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00027175 - PubMed: Guissart 2014 4-generation family, 3 affecteds (2F, M), unaffected heterozygous carrier parents - yes Turkey - - - - - Lichtenstein–Knorr syndrome see paper; early onset cerebellar ataxia, deafness 1 3 Johan den Dunnen
00027176 - PubMed: Guissart 2014 - - - France - - - - - ? individuals with ataxia and/or hearing loss 3 172 Johan den Dunnen
00301729 17-1731 PubMed: Maddirevula 2019 - F - - - - - - - ? ataxia and developmental delay. Her course has been static with slow improvement. She is ambulatory with recurrent falls. She has also cognitive delay particularly in language and learning. There is no history of seizures and no history of regression. Her brain MRI showed (at age 6) moderate cerebellar atrophy. MR spectroscopy was unremarkable. She underwent comprehensive metabolic testing which included CBC, renal profile, hepatic profile, lipid profile, transferrin, isoelectric focusing, CK, alpha fetoprotein, very long chain fatty acids, lactic acid, ammonia, tandem MS, biotinidase as well as urine organic acid and creatinine panel, all of which were normal. Her clinical exam is notable for axial and appendicular ataxia, and joint hyperlaxity. There were no pyramidal signs, dysmorphic features or nystagmus. 1 1 Johan den Dunnen
00314879 Trio48 PubMed: Zhu 2015 - F - United States - - - - - ? Microcephaly, minor dysmorphisms, profound developmental delays, epilepsy, gingival hypertrophy, microdontia, intracranial calcification of the basal ganglia, white matter abnormalities. 1 1 Johan den Dunnen
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