In this paper we present examples of man's identification of superiority with visual hyper-efficiency. From Babylonian, Egyptian, Minoan and Biblical times, the eye was the symbol of the master or the inspector. Similarly, a being or deity that was endowed with multiple eyes--with or without multiple heads--was considered to be extra powerful. An example is the crest of the British College of Optometrists, which is surmounted by a bird with three heads and hence supernumerary eyes, linking it to the College's motto 'aequis oculis videre' denoting equal vision. We present here photographic and textual data from several historical periods extending from the fourth millennium BC to the sixteenth century AD; and from different religious sources, both Christian and non-Christian, to support this thesis. However, these are only a few examples, selected from a larger on-going study of the subject.
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http://dx.doi.org/10.1111/j.1475-1313.1993.tb00503.x | DOI Listing |
Graefes Arch Clin Exp Ophthalmol
December 2024
Department of Ophthalmology, Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Kongjiang Road, No. 1665, Shanghai, 200092, China.
Purpose: To describe vascular anomalies and nonperfusion areas (NPAs) of stage 4 familial exudative vitreoretinopathy (FEVR) with radial retinal folds (RFs) and analyze their potential clinical significance.
Methods: Retinal detachment (RD) could exceed the RFs due to exudative, rhegmatogenous, or tractional factors, which we could call secondary RD. Fluorescein fundus angiography (FFA) and risk factors for progression to secondary RD of pediatric stage 4 FEVR patients with radial RFs were respectively explored.
BMC Pediatr
October 2024
School of Life Sciences, Bengbu Medical University, 2600 Donghai Avenue, Bengbu, 233000, China.
Background: Cat eye syndrome (CES) is a rare congenital disease frequently caused by a partial tetrasomy of the proximal long (q) arm of chromosome 22, due to a small supernumerary marker chromosome (sSMC). CES patients show remarkable phenotypic variability. Despite the progress of molecular cytogenetic technology, the cause of phenotypic variability and the genotype-phenotype correlations remain unknown.
View Article and Find Full Text PDFGenes (Basel)
August 2024
Institute of Medical and Molecular Genetics, Hospital Universitario La Paz, INGEMM-IdIPAZ, 28046 Madrid, Spain.
Orbit
August 2024
Govindram Seksaria Institute of Dacryology, L.V. Prasad Eye Institute, Hyderabad, India.
Congenital lacrimal drainage anomalies have several syndromic and non-syndromic associations reported in the literature. While the information is exhaustive, it may not be useful if someone wants to know the associations based on individual lacrimal anomalies quickly. For example, if someone wants to know the systemic associations of supernumerary punctum, it entails scanning of all the syndromes to note which of them reported the specific anomaly.
View Article and Find Full Text PDFChromosome Res
July 2024
Medical Genetic Diagnosis and Therapy Center, Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, No. 18 Daoshan Road, Gulou District, Fuzhou City, 350001, Fujian Province, China.
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