All individuals with variants in gene ASTN2

10 entries on 1 page. Showing entries 1 - 10.
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00000208 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), no prolactin deficiency, age sonographic determination testicular volume 17.64y, testicular volume right/left 21/20 (7.3–16ml) 1 1 Yu Sun
00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 2 1 Yu Sun
00213620 25351777-Pat1 PubMed: Nectoux 2015 3-generation family, 1 affected, unaffected parents M - France - - - - - LGMD progressive muscle weakness, difficulties in lifting weights, scapular winging and waddling gait; CPK 400; no intellectual disability 1 1 Juliette Nectoux
00213621 25351777-Fam2Pat2 PubMed: Nectoux 2015 2-generation family, 1 affected, unaffected parents M - France - - - - - LGMD late onset mild cognitive impairment 1 1 Aleksandra Nadaj Pakleza
00294730 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00307918 15DG0307 PubMed: Anazi 2017 family M - - - - - - - ID see paper; ..., abnormal facial shape; hypospadias; chordee; global developmental delay; depressed nasal bridge; frontal bossing; abnormality of the frontal hairline; microtia; anteverted nares; café au lait spot 1 1 Johan den Dunnen
00358960 Case28865 PubMed: Tiwari 2016 see paper M - Switzerland - - - - - retinal disease see paper; ... 1 1 LOVD
00358963 Case71762 PubMed: Tiwari 2016 see paper F - Switzerland - - - - - retinal disease see paper; ... 1 1 LOVD
00407658 J-60 PubMed: Kang 2016 - ? - Korea, South (Republic) - - - - - retinal disease end-stage renal disease (years): 1.2, extra-renal manifestations: OMA, optic nerve anomaly, cerebellar vermis aplasia, developmental delay, hepatic fibrosis, choledochal cyst 1 1 LOVD
00438591 HSC0040 PubMed: Hamdan 2017 WGS analysis 197 individuals with unexplained DEE (unaffected parents) - - Canada - - - - pharmaco-resistant seizures DEE - 1 1 Johan den Dunnen
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