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Heterotaxy and cardiac defect in a girl with chromosome translocation t(X;1)(q26;p13.1) and involvement of ZIC3
- Source :
- Eur J Hum Genet
- Publication Year :
- 2006
-
Abstract
- We report on a 2-year-old girl with situs ambiguus comprising right-sided stomach and spleen, left-sided liver and complex cardiac defect. Psychomotor development of this patient was normal, and no other major abnormalities were present. Chromosome analysis revealed a de novo balanced chromosome translocation t(X;1)(q26;p13.1). Molecular cytogenetic investigations identified a breakpoint spanning BAC clone on the X-chromosome containing the ZIC3 gene. Mutations in ZIC3 are associated with situs ambiguus and cardiac defects predominantly in males. This is the first report of a live born girl with an X-autosome translocation involving the ZIC3 region.
- Subjects :
- Pathology
medicine.medical_specialty
congenital, hereditary, and neonatal diseases and abnormalities
Heart Diseases
Heart malformation
Situs ambiguus
Chromosomal translocation
Spleen
Biology
Translocation, Genetic
Fetal Heart
Genetics
medicine
Humans
Gene
Genetics (clinical)
Homeodomain Proteins
Chromosomes, Human, X
Stomach
Breakpoint
Anatomy
medicine.disease
Radiography
medicine.anatomical_structure
Chromosomes, Human, Pair 1
Child, Preschool
Female
Heterotaxy
Transcription Factors
Subjects
Details
- ISSN :
- 10184813
- Volume :
- 14
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- European journal of human genetics : EJHG
- Accession number :
- edsair.doi.dedup.....c9c7690c0a1529775e822a1abd877a4f