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Lethal Congenital Contracture Syndrome Type 3 in an Isolated Canadian Population
Melissa J MacPherson1,2,3, Zachary C Nash4, Karen Y Niederhoffer1,2
1Department of Medical Genetics, University of Alberta, Edmonton, Alberta, Canada.
Diagnosing fetal akinesia deformation sequence (FADS) is difficult in isolated populations. This study identifies a novel PIP5K1C gene variant in three Canadian cases of lethal congenital contracture syndrome type 3 (LCCS3), suggesting a founder effect.
Area of Science:
- Genetics
- Medical Genetics
- Pediatric Genetics
Background:
- Prenatal diagnosis of fetal akinesia deformation sequence (FADS) is challenging, particularly in isolated populations with limited genetic data.
- Lethal congenital contracture syndromes type 3 (LCCS3) is an ultra-rare autosomal recessive disorder caused by PIP5K1C gene variants, with only 13 reported cases.
- Understanding the genetic basis of rare conditions in isolated communities is crucial for diagnosis and management.
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