| Literature DB >> 3934618 |
Abstract
Two cases with mental retardation, kyphosis, microcephalus, typical facial features, and eye anomalies had a previously undescribed recombinant chromosome change with duplication 2(q34; qter) secondary to paternal inversion 2(pter; q34). Eye findings consisted of reduced vision, myopia, nystagmus, iris defects and fundus lesions. Deformed optic discs were found in both patients and the retinal nerve fiber layer was thinner than normal.Entities:
Mesh:
Year: 1985 PMID: 3934618 DOI: 10.3109/13816818509006126
Source DB: PubMed Journal: Ophthalmic Paediatr Genet ISSN: 0167-6784