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  4. Ocular findings in a case of trisomy 18 with variant of dandy-walker syndrome
 
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Ocular findings in a case of trisomy 18 with variant of dandy-walker syndrome

Journal
Pediatrics and Neonatology
Date Issued
2010-10-01
Author(s)
PEN-HUA SU  
DOI
10.1016/S1875-9572(10)60056-3
URI
https://www.scopus.com/pages/publications/77958017485
https://scholars.csmu.edu.tw/handle/123456789/31313
Abstract
Trisomy 18 is the second most common chromosomal syndrome and has multiple dysmorphic features. However, ocular findings in trisomy 18 are rarely reported. Retinal folds are the most common ocular finding described to date, although retinal hypopigmentation, dysplasia, and areas of hemorrhage and gliosis are also found in trisomy 18. Dandy-Walker syndrome is a brain malformation that has been reported in association with numerous chromosomal abnormalities, although it has rarely been reported in association with trisomy 18. Here, we present a case of trisomy 18 with ocular pathology and variant of Dandy-Walker syndrome, a combination that has not previously been reported.
Type
journal article
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