Abstract
Treacher Collins syndrome is an autosomal dominant disorder of facial development, the features of which include conductive hearing loss and cleft palate. In the current investigation, linkage analysis has been used to make first trimester diagnostic predictions in a pregnancy at high risk of producing an affected child. The results of this analysis predicted that the child would be affected. As predictions of the severity of the disease were not possible, the pregnancy was also assessed by ultrasound imaging. This confirmed the affected diagnosis and predicted that the child would be severely affected.
MeSH Terms
Chromosome Aberrations/genetics
Chromosome Disorders
Electrophoresis, Polyacrylamide Gel
Female
Genes, Dominant/genetics
Genetic Linkage/genetics
Genetic Markers
Genotype
Humans
Infant
Infant, Newborn
Male
Mandibulofacial Dysostosis/diagnosis,genetics
Pedigree
Prenatal Diagnosis
Repetitive Sequences, Nucleic Acid/genetics
Translocation, Genetic/genetics
Ultrasonography
Chemicals
Genetic Markers
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Edwards S J
School of Biological Stlences, University of Manchester, UK.
Fowlie A
Cust M P
Liu D T
Young I D
Dixon M J
References (20)
20 references, click to expand
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