MG-105 Facial dysmorphism, skeletal abnormalities and central nervous system abnormalities in two sibs born to a consanguineous couple: A new autosomal recessive condition. (4th December 2015)

• Record Type: Journal Article
• Authors: Chad, Lauren; Thompson, Megan; Miron, Ioana; Shannon, Patrick; Keating, Sarah; Chitayat, David
• Is Part Of: Journal of medical genetics. Volume 52(2015)Supplement 1
• Page Start: A1
• Page End: A1
• Publication Date: 2015-12-04
• Subjects: Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmedgenet-2015-103577.1
• Languages: English
• ISSNs: 1468-6244

Abstract

Abstract : We report two female fetuses born to a consanguineous Sri-Lankan couple with facial dysmorphism, central nervous system and skeletal abnormalities. To our best knowledge this is a hitherto new autosomal recessive condition. The fetuses, both female, presented with thickened nuchal folds, echogenic bowel and kidneys, rocker-bottom feet, ventriculomegaly and intrauterine growth restriction. Detailed autopsies following termination of pregnancy at 23.4 and 22.3 weeks gestation respectively revealed short sloped forehead and hypertelorism with webbing of the neck, hydrocephalus with aqueduct stenosis as well as marked narrowing of the spinal canal and platyspondyly with delayed ossification and flattened acetabular roofs, broad hands with brachydactyly and narrow wrists. Microarray analysis was normal on both. These findings likely represent a new genetic syndrome with most probably autosomal recessive mode of inheritance. Whole genome sequencing is being done to try and identify the causative gene.