Ocular findings of albinism in DYRK1A- related intellectual disability syndrome

Ophthalmic Genet. 2020 Dec;41(6):650-655. doi: 10.1080/13816810.2020.1814349. Epub 2020 Aug 24.

Abstract

Background: Pathogenic variants in DYRK1A are associated with DYRK1A-related intellectual disability syndrome (DIDS). Common features of this diagnosis include microcephaly, intellectual disability, speech impairment, and distinct facial features. Reported ocular features include deep-set eyes, myopia, and strabismus. We present a case of DYRK1A-related intellectual disability syndrome with ocular findings of albinism and explore the possible pathogenesis of this previously unreported manifestation.

Materials and methods: This is a single, retrospective case report of a child with DIDS who underwent an ophthalmic exam including detailed visual electrophysiology. Results: A 21-month-old female with microcephaly, failure to thrive, language delay, cleft palate, and cardiac defects had an ophthalmic exam showing myopia, strabismus, a hypopigmented fundus and crossed asymmetry on visual evoked potential (VEP), consistent with ocular findings of albinism. Whole exome sequencing identified a pathogenic DYRK1A variant; no albinism gene variants were reported. Her constellation of features is consistent with a diagnosis of DYRK1A-related intellectual disability syndrome; however, ocular features of albinism have not previously been reported in this condition.

Conclusions: This is, to the best of our knowledge, the first report of ocular findings of albinism in a case of DYRK1A-related intellectual disability syndrome. We propose that ocular albinism is a novel ocular phenotype of DYRK1A-related disease. Ophthalmic exams in patients with this diagnosis should include thorough evaluation for ocular albinism, including VEPs.

Keywords: DYRK1A; albinism; intellectual disability; visual evoked potential; whole exome sequencing.

Publication types

  • Case Reports

MeSH terms

  • Albinism / complications
  • Albinism / genetics
  • Albinism / pathology*
  • Dyrk Kinases
  • Evoked Potentials, Visual
  • Female
  • Haploinsufficiency*
  • Humans
  • Infant
  • Intellectual Disability / complications
  • Intellectual Disability / genetics
  • Intellectual Disability / pathology*
  • Protein Serine-Threonine Kinases / genetics*
  • Protein-Tyrosine Kinases / genetics*
  • Retrospective Studies
  • Syndrome

Substances

  • Protein-Tyrosine Kinases
  • Protein Serine-Threonine Kinases