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620327.1.3
Home
Subject Details
Country
Saudi Arabia; Yemen
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Sex
Male
Subject Variants
Variant Name
Allele Count
NM_001001683.4:c.325C>T
1
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Remarks
Father of 620327.1.1
References
Calì et al. 2022
Related Subjects
Subject Id
Country
HPO Terms
Sex
Family History
Parental Consanguinity
Remarks
620327.1.1
Saudi Arabia; Yemen
Neonatal respiratory distress; Hypotonia; Global developmental delay; Myoclonic seizure; Dysgyria; Cerebellar hypoplasia; Cerebellar atrophy; Nystagmus; Abnormal facial shape; Patent ductus arteriosus; Atrial septal defect; Bilateral cryptorchidism; Abnormality of the kidney
Male
Yes
Yes
Patient from "family B" in the publication
620327.1.2
Saudi Arabia; Yemen
Neonatal respiratory distress; Hypotonia; Abnormal facial shape; Atrial septal defect; Bilateral cryptorchidism; Exaggerated startle response; Dysgyria; Cerebellar atrophy; Inferior cerebellar vermis hypoplasia; Cerebral white matter hypoplasia; Hydronephrosis
Male
Yes
Yes
Brother of 620327.1.1
620327.1.4
Saudi Arabia; Yemen
Female
Mother of 620327.1.1
Back to search Result
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العربية
About Us
News
Fellowships
العربية
Home
About Us
CTGA Database
CTGA Overview
Search Database
Submit to Database
Publications
Research Articles
Genetics Made Easy
Genetic Disorders in the Arab World
Reports
Conferences & Events
News
Gallery
Fellowships
Contact Us