610188.4

Country

United Arab Emirates

HPO Terms

Global developmental delay; Intellectual disability; Seizure; Abnormal posterior cranial fossa morphology
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Sex

Female

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_025114.3:c.4792_4795del2

Remarks

Affected sibling

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
610188.5United Arab EmiratesGeneralized hypotonia; Global developmental delay; Visual impairment; NystagmusFemaleYes
610188.6United Arab EmiratesRetinal dystrophy; Nephronophthisis; Molar tooth sign on MRIFemaleYes
610188.7United Arab EmiratesGlobal developmental delay; Molar tooth sign on MRIFemaleYesYes
610188.8United Arab EmiratesGlobal developmental delay; Molar tooth sign on MRIFemaleYesYes
610188.9United Arab EmiratesMolar tooth sign on MRIUnknown
610188.10United Arab EmiratesMolar tooth sign on MRI; NephronophthisisUnknown
610188.11United Arab EmiratesAtaxia; Molar tooth sign on MRI; Global developmental delay; HypotoniaUnknownYesPatient from 'JS_F11' family in the publication
610188.12United Arab EmiratesAtaxia; Molar tooth sign on MRI; Global developmental delay; HypotoniaUnknownYesPatient from 'MTI_587' family in the publication
610188.13United Arab EmiratesAtaxia; Molar tooth sign on MRI; Global developmental delay; HypotoniaUnknownYesPatient from 'MTI_012' family in the publication
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