Usher syndrome

An effective sequencing approach to establish a genetic and clinical diagnosis

S. Lenarduzzi, Diego Vozzi, A. Morgan, E. Rubinato, A. D'Eustacchio, T. M. Osland, C. Rossi, C. Graziano, P. Castorina, U. Ambrosetti, M. Morgutti, G. Girotto

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

Usher syndrome is an autosomal recessive disorder characterized by retinitis pigmentosa, sensorineural hearing loss and, in some cases, vestibular dysfunction. The disorder is clinically and genetically heterogeneous and, to date, mutations in 11 genes have been described. This finding makes difficult to get a precise molecular diagnosis and offer patients accurate genetic counselling. To overcome this problem and to increase our knowledge of the molecular basis of Usher syndrome, we designed a targeted resequencing custom panel. In a first validation step a series of 16 Italian patients with known molecular diagnosis were analysed and 31 out of 32 alleles were detected (97% of accuracy). After this step, 31 patients without a molecular diagnosis were enrolled in the study. Three out of them with an uncertain Usher diagnosis were excluded. One causative allele was detected in 24 out 28 patients (86%) while the presence of both causative alleles characterized 19 patients out 28 (68%).Sixteen novel and 27 known alleles were found in the following genes: USH2A (50%), MYO7A (7%), CDH23 (11%), PCDH15 (7%) and USH1G (2%). Overall, on the 44 patients the protocol was able to characterize 74 alleles out of 88 (84%).These results suggest that our panel is an effective approach for the genetic diagnosis of Usher syndrome leading to: 1) an accurate molecular diagnosis, 2) better genetic counselling, 3) more precise molecular epidemiology data fundamental for future interventional plans.

Original languageEnglish
Pages (from-to)18-23
Number of pages6
JournalHearing Research
Volume320
DOIs
Publication statusPublished - 1 Feb 2015
Externally publishedYes

Fingerprint

Usher Syndromes
Alleles
Genetic Counseling
Retinitis Pigmentosa
Molecular Epidemiology
Sensorineural Hearing Loss
Genes
Mutation

ASJC Scopus subject areas

  • Sensory Systems
  • Medicine(all)

Cite this

Lenarduzzi, S., Vozzi, D., Morgan, A., Rubinato, E., D'Eustacchio, A., Osland, T. M., ... Girotto, G. (2015). Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis. Hearing Research, 320, 18-23. https://doi.org/10.1016/j.heares.2014.12.006

Usher syndrome : An effective sequencing approach to establish a genetic and clinical diagnosis. / Lenarduzzi, S.; Vozzi, Diego; Morgan, A.; Rubinato, E.; D'Eustacchio, A.; Osland, T. M.; Rossi, C.; Graziano, C.; Castorina, P.; Ambrosetti, U.; Morgutti, M.; Girotto, G.

In: Hearing Research, Vol. 320, 01.02.2015, p. 18-23.

Research output: Contribution to journalArticle

Lenarduzzi, S, Vozzi, D, Morgan, A, Rubinato, E, D'Eustacchio, A, Osland, TM, Rossi, C, Graziano, C, Castorina, P, Ambrosetti, U, Morgutti, M & Girotto, G 2015, 'Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis', Hearing Research, vol. 320, pp. 18-23. https://doi.org/10.1016/j.heares.2014.12.006
Lenarduzzi, S. ; Vozzi, Diego ; Morgan, A. ; Rubinato, E. ; D'Eustacchio, A. ; Osland, T. M. ; Rossi, C. ; Graziano, C. ; Castorina, P. ; Ambrosetti, U. ; Morgutti, M. ; Girotto, G. / Usher syndrome : An effective sequencing approach to establish a genetic and clinical diagnosis. In: Hearing Research. 2015 ; Vol. 320. pp. 18-23.
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