223800.7

Country

Egypt

HPO Terms

Seizure ; Short stature; Brachydactyly; Camptodactyly; Hyperlordosis; Platyspondyly
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Sex

Female

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_017653.6:c.610C>T2NA

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
223800.3EgyptPostnatal growth retardation; Microcephaly; Abnormal facial shape; Abnormal thorax morphology; Scoliosis; Rhizomelia; Intellectual disability; Platyspondyly; Epiphyseal dysplasia; Metaphyseal dysplasia; Iliac crest serrationUnknownNoPatient from Family 9 in the publication. The same patient was described in a previous locus homozygosity mapping study.
223800.6EgyptGlobal developmental delay; Short stature; ScoliosisMaleYes
223800.10EgyptIntellectual disability; Short stature; Short neck; Pectus excavatum; Intercostal retractionsYesYes
223800.11EgyptSkeletal dysplasiaMalePatient's parents are from the same region.
223800.12EgyptIntellectual disability; Abnormality of the vertebral column; MicrocephalyMaleYesYes
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