Expanding the clinical spectrum and management of Traboulsi syndrome: report on two siblings homozygous for a novel pathogenic variant in ASPH. (4th July 2021)

• Record Type: Journal Article
• Authors: Van Hoorde, Tom; Nerinckx, Fanny; Kreps, Elke; Roels, Dimitri; Huyghe, Philippe; Van Heetvelde, Mattias; Verdin, Hannah; De Baere, Elfride; Balikova, Irina; Leroy, Bart P.
• Is Part Of: Ophthalmic genetics. Volume 42:Number 4(2021)
• Page Start: 493
• Page End: 499
• Publication Date: 2021-07-04
• Subjects: Traboulsi syndrome -- novel pathogenic variant -- ASPH -- exon 25 -- homozygous -- consanguinity -- spontaneous filtering blebs -- clear lens extraction -- rigid gas-permeable contact lenses; Eye -- Diseases -- Genetic aspects -- Periodicals; Eye Diseases -- genetics -- Periodicals; Eye Diseases -- in infancy & childhood -- Periodicals; 617.7
• DOI: 10.1080/13816810.2021.1923039
• Languages: English
• ISSNs: 1381-6810

Abstract

ABSTRACT: Background: Traboulsi syndrome is a very rare, syndromic form of ectopia lentis that is potentially sight-threatening at a young age. It is characterized by typical facial, skeletal and ocular signs. Materials and Methods: Two siblings, born to consanguineous parents, with a clinical phenotype consistent with Traboulsi syndrome, underwent extensive ophthalmic imaging and exome-based genetic testing. Both were treated with unilateral clear lens extraction via a limbal approach. Results: Two siblings, one male and one female, presented with systemic and ocular features consistent with Traboulsi syndrome. Lens subluxation was present in all 4fouraffected eyes, and spontaneous subconjunctival bleb formation was detected in one eye. This eye also showed evidence of keratoconus-related corneal thinning. The clinical diagnosis of Traboulsi syndrome was confirmed molecularly. A homozygous, novel, pathogenic nonsense variant was identified in exon 25 of the ASPH gene: c.2181_2183dup, p.(Val727_Trp728insTer). Excellent visual outcomes following clear lens extraction and postoperative rigid gas-permeable contact lens fitting were obtained. Conclusions: We expanded the genetic spectrum of Traboulsi syndrome with a novel frameshift variant in the ASPH gene. We showed that lensectomy followed by gas-permeable contact lenses is an efficient therapeutic approach to treat lens subluxation in Traboulsi syndrome. However, lifelong follow-up is crucial to avoid (late) postoperative complications.