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PMID: 8818950 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't

Prenatal diagnosis in Treacher Collins syndrome using combined linkage analysis and ultrasound imaging.

Journal of medical genetics ·Vol. 33 ·No. 7 ·1996-07-00 ·Pages 603-6

Edwards SJ, Fowlie A, Cust MP, Liu DT, Young ID, Dixon MJ

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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Article Info
Journal
Journal of medical genetics
Abbr.
J Med Genet
ISSN
0022-2593
Published
1996-07-00
Pages
603-6
Language
English
Region
England
NLM ID
2985087R
PMCID
PMC1050672
Subset
IM
Grants
Wellcome Trust · United Kingdom
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