HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Cerebral visual impairment in CDKL5 deficiency disorder: vision as an outcome measure.

AbstractAIM:
To characterize the neuro-ophthalmological phenotype of cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) and assess visual acuity as a reproducible, quantitative outcome measure.
METHOD:
We retrospectively analyzed clinical data from patients with CDD. Complete neuro-ophthalmological assessments, including visual acuity, were evaluated.
RESULTS:
Of 26 patients (22 females, four males; median age 4y, interquartile range 2y 1mo-7y 10mo), cerebral visual impairment (CVI), defined as visual dysfunction in the absence of ocular or anterior visual pathway abnormalities, was diagnosed in all those over 2 years of age. Ophthalmological examinations revealed nystagmus in 10 patients and strabismus in 24 patients. Visual acuity was measured in 24 patients, by preferential looking in all and by sweep visual evoked potential in 13. Visual acuities were lower than age expectations and demonstrated improvement in the first 3 years. Adjusting for age and sex, average preferential looking visual acuity after 2 years of age was higher in patients with intact mobility than in those who were non-mobile.
INTERPRETATION:
CVI was observed in patients with CDD. Visual acuity improved over time and correlated with mobility. Visual acuity, as a quantifiable measure of visual function, should be considered as an outcome measure in pre-clinical and clinical studies for CDD. What this paper adds Cerebral visual impairment is highly prevalent in cyclin-dependent kinase-like 5 deficiency disorder (CDD). Visual acuity is a measurable quantitative outcome measure in CDD. Visual acuity in CDD correlates with gross motor ability.
AuthorsHeather E Olson, Julia G Costantini, Lindsay C Swanson, Walter E Kaufmann, Timothy A Benke, Anne B Fulton, Ronald Hansen, Annapurna Poduri, Gena Heidary
JournalDevelopmental medicine and child neurology (Dev Med Child Neurol) Vol. 63 Issue 11 Pg. 1308-1315 (11 2021) ISSN: 1469-8749 [Electronic] England
PMID34028805 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Copyright© 2021 Mac Keith Press.
Topics
  • Child
  • Child, Preschool
  • Epileptic Syndromes (genetics, physiopathology)
  • Evoked Potentials, Visual (physiology)
  • Female
  • Humans
  • Male
  • Phenotype
  • Retrospective Studies
  • Spasms, Infantile (genetics, physiopathology)
  • Vision Disorders (genetics, physiopathology)
  • Vision, Ocular (physiology)
  • Visual Pathways (physiopathology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: