Progressive brain atrophy and severe neurodevelopmental phenotype in siblings with biallelic COASY variants.
Justin RosatiJessica JohnsonZinandre StanderAmy WhiteSilvia TortorelliDiana BaileyChin-To FongBo Hoon LeePublished in: American journal of medical genetics. Part A (2022)
Biallelic pathogenic variants in the COASY gene have been associated with two distinct disease phenotypes, that is, COASY-protein associated neurodegeneration (CoPAN) and pontocerebellar hypoplasia type 12 (PCH 12). We present two siblings that independently presented with significant hypotonia and respiratory insufficiency at birth. Comprehensive genetic testing revealed homozygous variants within COASY, however, the progressive clinical and neuroradiologic findings described here are unique and have not been described previously. Magnetic resonance imaging showed progressive diffuse parenchymal loss throughout the bilateral cerebral hemispheres and atrophy of the basal ganglia and brainstem. As such, this article brings forth two additional cases of COASY-related disorder with abnormal newborn screening acylcarnitine profiles resembling carnitine palmitoyl transferase 1a (CPT1a) deficiency in two siblings who presented at birth with contractures, marked hypotonia and absent respiratory drive.
Keyphrases
- intellectual disability
- copy number
- multiple sclerosis
- magnetic resonance imaging
- autism spectrum disorder
- genome wide
- white matter
- gestational age
- computed tomography
- early onset
- subarachnoid hemorrhage
- low grade
- respiratory tract
- gene expression
- magnetic resonance
- binding protein
- transcription factor
- pregnant women
- cerebral ischemia
- amino acid
- drug induced
- pregnancy outcomes
- contrast enhanced
- replacement therapy
- blood brain barrier
- small molecule
- congenital heart disease
- genome wide identification