Anirdia-like phenotype caused by 6p25 dosage aberrations
Karthikeyan Arcot Sadagopan1, Grace T Liu, Jenina E Capasso
1Ocular Genetics, Wills Eye Institute, Philadelphia, Pennsylvania; Department of Pediatric Ophthalmology, Strabismus and Ocular Genetics, Ocular Genetics Service, Aravind Eye Hospital, Madurai, India.
American Journal of Medical Genetics. Part A
|February 19, 2015
Summary
Axenfeld-Rieger spectrum and aniridia-like phenotypes can be caused by genetic changes on chromosome 6p25. Chromosomal microarray analysis helps differentiate these conditions, crucial for prognosis and treatment.
Area of Science:
- Ophthalmology
- Genetics
- Developmental Biology
Background:
- Axenfeld-Rieger spectrum (ARS) is a group of anterior segment dysgeneses often leading to glaucoma in children.
- ARS is frequently associated with mutations in FOXC1 or PITX2 transcription factors, critical for anterior segment development.
- Classic aniridia, a pan-ophthalmic disorder, results from PAX6 gene mutations and can involve optic nerve hypoplasia and Wilms tumor.
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