All individuals with variants in gene SLC39A5

4 entries on 1 page. Showing entries 1 - 4.
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00000070 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00300239 HM736 PubMed: Liu 2020 - M - China - - - - - MYP onset early childhood; refraction spherical equivalent OD –8.00, OS –20.50 1 1 Johan den Dunnen
00379707 R0020 PubMed: Wan 2018 - ? - China Han Chinese - - - - retinal disease - 1 1 LOVD
00419899 Pat16 PubMed: Angelozzi 2022 2-generation family, 1 affected, mildly affected mother M - - - - - - - MYP, NDD birth 40w; no IUGR; failure to thrive; picky eating, weight loss; hypotonia; global developmental delay; gross motor delay; fine motor delay; 10-11m-sit; 36m-walk; speech delay, 11m-first words; intellectual disability, IQ not formally assessed by neuropsychologist; behavioral problems; no hyperactivity/ADHD; no anxiety; no microcephaly; MRI brain normal; EEG normal; headaches with emesis 2-3 days a week; Prescribed glasses, presumably because of myopia; no strabismus; normal hearing; broad forehead, small palpebral fissures, triangular face with pointed chin, low-set and posteriorly rotated ears; skin lesions (tags vs nevi); 5y-poor dentition with pulpectomy and crowns; slender fingers with broader thumbs and halluxes, prominent heels; no ventricular septal defect; no atrial septal defect; no patent foramen; no vascular anomalies; no gastrointestinal findings; no genitourinary findings 1 1 Johan den Dunnen
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