| Literature DB >> 27018276 |
Pinar Altiaylik Ozer1, Emrah Utku Kabatas2, Bengi Ece Kurtul2, Cigdem Seher Kasapkara3.
Abstract
A full-term infant with neonatal seizures was diagnosed to have corpus callosum agenesis with congenital agyria. His indirect ophthalmoscopical evaluation revealed bilateral complete absence of retinal vessels with normal optic discs and macula. Bilateral lamellar cataracts developed in the second month of follow-up, and his muscle biopsy was consistent with a mitochondrial disorder. Confirmation by molecular analysis could not be performed since parents did not give their consent for further investigation.Entities:
Keywords: Central nervous system; Developmental abnormality; Retinal vascular agenesis
Mesh:
Year: 2016 PMID: 27018276 DOI: 10.1007/s10792-016-0224-5
Source DB: PubMed Journal: Int Ophthalmol ISSN: 0165-5701 Impact factor: 2.031