251450.3

Country

Syria

HPO Terms

Skeletal dysplasia; Low-set ears; Abnormality of the outer ear; Narrow nasal bridge
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Sex

Female

Family History

Yes

Parental Consanguinity

Yes

Subject Variants

Variant NameAllele CountAllele FrequencyAssociated DiseaseAssociated Gene
NM_001159773.2:c.902_906dup2NA

Related Subjects

Subject IdCountryHPO TermsSexFamily HistoryParental ConsanguinityRemarks
251450.1SyriaSkeletal dysplasia; Macrocephaly at birth; Short stature; Wide anterior fontanelMaleYes
251450.2SyriaBrachydactyly; Acromelia; Bilateral talipes equinovarus; Micrognathia; Narrow palpebral fissureFemaleYesYes
251450.5SyriaSevere short stature; Multiple joint dislocationFemaleYes
251450.6SyriaLimb undergrowth; Narrow chest; Neonatal respiratory distress; Round face; MicrognathiaMaleYes
251450.7SyriaIntrauterine growth retardation; Large joint dislocations; Monkey wrench femoral neck; Talipes equinovarus; Radial club hand; Therapeutic abortionNoYes
251450.8SyriaGrowth delay; Joint dislocation; Abnormality of the hand; Retrognathia; GlaucomaYes
251450.9SyriaGrowth delay; Joint dislocation; Bifid distal phalanx of the thumb; Talipes equinovarus; Narrow chest; Craniosynostosis; Patent foramen ovale; Patent ductus arteriosusYes
251450.10SyriaIntellectual disability; Hyperlordosis; Joint dislocationMaleYesPatient from 'family 7' in the publication
251450.11SyriaJoint dislocation; Death in infancyMaleYesPatient from 'family 8' in the publication
251450.12SyriaSkeletal dysplasiaYesFetus
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