Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless
- Author(s)
- Wallis, M; Bodek, SD; Munro, J; Rafehi, H; Bennett, MF; Ye, Z; Schneider, A; Gardiner, F; Valente, G; Murdoch, E; Uebergang, E; Hunter, J; Stutterd, C; Huq, A; Salmon, L; Scheffer, I; Eratne, D; Meyn, S; Fong, CY; John, T; Mullen, S; White, SM; Brown, NJ; McGillivray, G; Chen, J; Richmond, C; Hughes, A; Krzesinski, E; Fennell, A; Chambers, B; Santoreneos, R; Le Fevre, A; Hildebrand, MS; Bahlo, M; Christodoulou, J; Delatycki, M; Berkovic, SF;
- Details
- Publication Year 2024-08-02,Volume 19,Issue #1,Page 288
- Journal Title
- Orphanet Journal of Rare Diseases
- Abstract
- BACKGROUND: Significant recent efforts have facilitated increased access to clinical genetics assessment and genomic sequencing for children with rare diseases in many centres, but there remains a service gap for adults. The Austin Health Adult Undiagnosed Disease Program (AHA-UDP) was designed to complement existing UDP programs that focus on paediatric rare diseases and address an area of unmet diagnostic need for adults with undiagnosed rare conditions in Victoria, Australia. It was conducted at a large Victorian hospital to demonstrate the benefits of bringing genomic techniques currently used predominantly in a research setting into hospital clinical practice, and identify the benefits of enrolling adults with undiagnosed rare diseases into a UDP program. The main objectives were to identify the causal mutation for a variety of diseases of individuals and families enrolled, and to discover novel disease genes. METHODS: Unsolved patients in whom standard genomic diagnostic techniques such as targeted gene panel, exome-wide next generation sequencing, and/or chromosomal microarray, had already been performed were recruited. Genome sequencing and enhanced genomic analysis from the research setting were applied to aid novel gene discovery. RESULTS: In total, 16/50 (32%) families/cases were solved. One or more candidate variants of uncertain significance were detected in 18/50 (36%) families. No candidate variants were identified in 16/50 (32%) families. Two novel disease genes (TOP3B, PRKACB) and two novel genotype-phenotype correlations (NARS, and KMT2C genes) were identified. Three out of eight patients with suspected mosaic tuberous sclerosis complex had their diagnosis confirmed which provided reproductive options for two patients. The utility of confirming diagnoses for patients with mosaic conditions (using high read depth sequencing and ddPCR) was not specifically envisaged at the onset of the project, but the flexibility to offer recruitment and analyses on an as-needed basis proved to be a strength of the AHA-UDP. CONCLUSION: AHA-UDP demonstrates the utility of a UDP approach applying genome sequencing approaches in diagnosing adults with rare diseases who have had uninformative conventional genetic analysis, informing clinical management, recurrence risk, and recommendations for relatives.
- Publisher
- BMC
- Keywords
- Humans; Adult; Female; Male; Australia; *Rare Diseases/genetics/diagnosis; Undiagnosed Diseases/genetics/diagnosis; Genetic Testing/methods; Middle Aged; Young Adult; Nars; Prkacb; Top3b; Genome sequencing; Genotype; Mosaicism; Phenotype; Rare disease; Tuberous sclerosis; Undiagnosed disease
- Research Division(s)
- Population Health And Immunity
- PubMed ID
- 39095811
- Publisher's Version
- https://doi.org/10.1186/s13023-024-03297-5
- Open Access at Publisher's Site
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Creation Date: 2024-08-14 09:49:49
Last Modified: 2024-08-14 11:28:32