613763.1.7

Country

Saudi Arabia
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Sex

Female

Family History

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001289808.2:c.166C>T2

Remarks

Mother of 6137673.1.1. Examination revealed "visually insignificant lens opacities and a tessellated fundus with moderate myopia in her left eye" while her "ERG showed mildly depressed rod and cone function".

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
613763.1.1Saudi ArabiaDevelopmental cataract; Congenital aphakia; Retinal dystrophyFemaleYesYesPatient had cataract surgery as an infant and left aphakic resulting in later retinal degeneration
613763.1.2Saudi ArabiaDevelopmental cataract; Congenital aphakia; Retinal dystrophyFemaleYesYesSister of 6137673.1.1. Patient had cataract surgery as an infant and left aphakic resulting in later retinal degeneration
613763.1.3Saudi ArabiaDevelopmental cataract; Congenital aphakia; Retinal detachmentFemaleYesYesDaughter of 6137673.1.1. Patient had cataract surgery at 16 months of age
613763.1.4Saudi ArabiaNuclear cataract; PseudophakiaFemaleYesYesDaughter of 6137673.1.1. Patient had cataract surgery at 16 months of age
613763.1.5Saudi ArabiaFemaleYesYesDaughter of 6137673.1.1. Asymptomatic but slit-lamp examination revealed 'visually insignificant lens (nuclear and cortical) opacities"
613763.1.6Saudi ArabiaMaleYesYesSon of 6137673.1.1. Asymptomatic but retinoscopy revealed "clinically insignificant fine opacities in the red reflect".
613763.1.8Saudi ArabiaMaleHusband (and first-cousin) of 6137673.1.1.
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