| Autor: |
Thales A. C De Guimarães, Jenina E Capasso, Nicholas R Bello, Nutsuchar Wangtiraumnuay, Michelle D Lingao, Wadakarn Wuthisiri, Yu-Hung Lai, Erica S Johnson, Mario Zanolli, Vikas Khetan, Renu Bajaj, Zi-Xuan Wang, Stephen C Peiper, Alex V Levin |
| Jazyk: |
angličtina |
| Rok vydání: |
2021 |
| Předmět: |
|
| Zdroj: |
The Pan-American Journal of Ophthalmology, Vol 3, Iss 1, Pp 10-10 (2021) |
| Druh dokumentu: |
article |
| ISSN: |
2666-4909 |
| DOI: |
10.4103/pajo.pajo_63_20 |
| Popis: |
Introduction: The etiologies of congenital and developmental cataracts are diverse. Most are not syndromic and have no identifiable cause, thus creating a diagnostic dilemma. We investigated the utility of chromosomal microarray in identifying the etiology of isolated childhood cataracts. Methods: Patients with congenital or developmental cataracts without other associated abnormalities received a single-nucleotide polymorphism (SNP) microarray. copy number variations (CNV) and regions of homozygosity (ROH) were compared with previous literature reports and analyzed for candidate genes to assess pathogenicity. Results: We enrolled 37 patients. The mean age of the patient population was 10.98 years old. Nineteen patients (51.4%) had bilateral cataract. Positive family history was found in 11 patients (29.7%). Eighteen patients (48.7%) had a variant on microarray: 10 (27%) with CNV, 5 (13.5%) with ROH, and 3 patients (8.1%) with both CNV and homozygosity. In five patients (13.5%), we found a potentially causative cataract gene within an ROH. Discussion: There is a high rate of notable findings among the CNV and ROH detected. Three patients were homozygous in a region known to have a cataract gene suggesting a possible autosomal recessive disease. In those with CNV, segregation would help to affirm the pathogenicity of these regions and may lead to the identification of new genes. Conclusion: SNP microarray had a surprisingly high rate of notable findings in patients with isolated cataract and may reveal the opportunities for genetic counseling, lead to discovering new cataract genes and identify additional affected genes that could lead to other clinical abnormalities. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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