253260.8

Country

United Arab Emirates

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001370658.1:c.1535C>T1
NM_001370658.1:c.262A>G1

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
253260.5United Arab EmiratesDelayed speech and language development; Specific learning disabilityMaleYesYesAffected brother
253260.6United Arab EmiratesStrabismus; Delayed speech and language development; Hyperpigmented/hypopigmented macules; Hearing impairmentMaleYesYesSibling with hyperactivity
253260.7United Arab EmiratesDecreased biotinidase levelMaleYesYesInfant with double homozygous BTD variants contributing to profound biotinidase deficiency. He has a brother with speech delay and absent serum biotinidase activity (no molecular test).
253260.9United Arab EmiratesGlobal developmental delay; Seizure; Blindness; Sleep disturbance; Hearing impairmentMaleNoYes
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