All individuals with variants in gene MCOLN1

7 entries on 1 page. Showing entries 1 - 7.
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00000082 - PubMed: Bell 2011 - - - - - - - - - - - 2 1 Global Variome, with Curator vacancy
00050454 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? optic atrophy, global developmental delay, seizures, obesity, cerebellar atrophy, generalized neonatal hypotonia, hypothyroidism, hypsarrhythmia 2 1 Johan den Dunnen
00361604 11DG0141 PubMed: Anazi 2017 simplex case F yes Saudi Arabia - - - - - ID syndromic; global developmental delay, hazy cornea, brain dysmyelination 1 1 Johan den Dunnen
00388555 OFTALMO.016 PubMed: Dineiro 2020 - ? - Spain - - - - - retinal disease Hidden syndrome 1 1 LOVD
00395595 RP-2032 PubMed: Perea-Romero 2021 - - - Spain - - - - - retinal disease astigmatism, corneal dystrophy, dyschromatopsia, hypermetropia, photophobia, rod-cone dystrophy, hearing impairment, abnormal serum iron, intellectual disability, moderate 1 1 LOVD
00428058 Pat62346;R64921 PubMed: Kumar 2022, PubMed: Yepez 2022 2-generation family, 1 affected, unaffected parents M no France - - - - - ? see paper; ..., normal pregnancy, delivery, birth; early psychomotor development normal; deleayed speech development, 4y-language; 11y-psychomotor regression, progressive visual loss, degenerative retinopathy, cerebellar ataxia, hyperreflexia, external ophthalmoparesis, bilateral corneal clouding, abnormal behavior; muscle biopsy moderate subsarcolemmal accumulation mitochondria; 47y-severe walking difficulties, ataxia, blindness, cerebellar ataxia, hyperreflexia, external ophthalmoparesis predominating in vertical gaze, bilateral corneal clouding, abnormal behavior (easily frightened, sometimes aggressive; spontaneous speech markedly reduced 2 1 Johan den Dunnen
00466473 - - - M yes Morocco - - - - - ML4 Vitreoretinopathy, Delayed speech and language development, Hearing impairment, Hypotonia, Motor delay, achlorhydria, anaemia, 1 1 Maria Elena García Paya
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