228520.1.2

Country

Saudi Arabia

HPO Terms

Hypertelorism; Midface retrusion; Lens subluxation; High myopia; Sensorineural hearing impairment; Thickened calvaria; Platyspondyly; Atlantoaxial abnormality; Cataract; Retinal detachment; Visual loss; Accelerated skeletal maturation
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Sex

Male

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001854.3:c.2702G>A2NA

Remarks

Patient 2 in the publication, brother of 228520.1.1

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
228520.1.1Saudi ArabiaHypertelorism; Midface retrusion; Wide nasal bridge; Long philtrum; High myopia; Iridodonesis; Lens subluxation; Sensorineural hearing impairment; Thickened calvaria; Platyspondyly; Expressive language delay; Atlantoaxial abnormalityMaleYesYesPatient 1 in the publication
228520.1.3Saudi ArabiaMild short stature; Thickened calvariaUnknownYesYesSibling of 228520.1.1, mild phenotype noted
228520.1.4Saudi ArabiaMild short stature; Thickened calvariaUnknownYesYesSibling of 228520.1.1, mild phenotype noted
228520.1.5Saudi ArabiaMixed hearing impairment; Mild short stature; Thickened calvariaMaleFather of 228520.1.1, mild phenotype noted
228520.1.6Saudi ArabiaMixed hearing impairment; Mild short stature; Thickened calvariaFemaleMother of 228520.1.1, mild phenotype noted
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