Genome sequencing identifies biallelic variants in SCLT1 in a patient with syndromic nephronophthisis: Reflections on the SCLT1-related ciliopathy spectrum.
E GillesseA WadeJ S ParboosinghP Y B AuF P Berniernull nullR E LamontA Micheil InnesPublished in: American journal of medical genetics. Part A (2024)
Ciliopathies represent a major category of rare multisystem disease. Arriving at a specific diagnosis for a given patient is challenged by the significant genetic and clinical heterogeneity of these conditions. We report the outcome of the diagnostic odyssey of a child with obesity, renal, and retinal disease. Genome sequencing identified biallelic splice site variants in sodium channel and clathrin linker 1 (SCLT1), an emerging ciliopathy gene. We review the literature on all patients reported with biallelic SCLT1 variants highlighting a frequent clinical presentation that overlaps Bardet-Biedl and Senior-Loken syndromes. We also discuss current concepts in syndrome designation in light of these data.
Keyphrases
- copy number
- genome wide
- intellectual disability
- case report
- single cell
- end stage renal disease
- dna methylation
- newly diagnosed
- ejection fraction
- chronic kidney disease
- autism spectrum disorder
- type diabetes
- systematic review
- insulin resistance
- peritoneal dialysis
- prognostic factors
- optical coherence tomography
- weight gain
- gene expression
- electronic health record
- big data
- adipose tissue
- skeletal muscle
- high fat diet induced
- physical activity