Analysis of macular, foveal, and retinal nerve fiber layer thickness in children with unilateral anisometropic amblyopia and their changes following occlusion therapy

Purpose: To analyze macular thickness (MT), foveal thickness (FT), and retinal nerve fibre layer thickness (RNFLT) in children with unilateral anisometropic amblyopia and their changes following occlusion therapy. Methods: A prospective, longitudinal, and comparative study of 60 children aged between 5 and 18 years consisted of two groups, group 1: 30 children with unilateral anisometropic amblyopia; group 2: 30 normal children. Best corrected visual acuity (BCVA), a detailed ocular examination, spectral domain optical coherence tomography for MT, FT, and RNFLT in both eyes were done at visit one (baseline) and every 3 months for a year following occlusion therapy (initiated one month after first visit) in group 1. Results: Mean BCVA, MT, FT, and RNFLT in amblyopic eyes at first visit were 0.63 ± 0.405, 286.9 ± 6.522 ?m, 195.90 ± 8.462 ?m, and 100.87 ± 6.240 ?m, respectively and at last visit after occlusion therapy were 0.50 ± 0.318, 248.9 ± 11.681 ?m, 169.47 ± 10.941 ?m, and 99.43 ± 5.722 ?m, respectively. At first visit, mean BCVA, MT, FT, and RNFLT in nonamblyopic eyes (group 1) were 0 ± 0, 240 ± 10.447 ?m, 159.27 ± 9.285 ?m, 98.63 ± 4.723 ?m and in normal eyes (group 2: average of right and left eyes) were 0 ± 0, 239.8 ± 4.294 ?m, 143.6 ± 4.61 ?m, 100.5 ± 2.895 ?m, respectively. Conclusion: MT and FT, which were more in amblyopic eyes as compared to normal fellow eyes and group 2, decreased with improvement in BCVA after occlusion therapy. However, there was no difference in RNFLT between amblyopic eyes and normal fellow eyes and group 2 before and after occlusion therapy.

Sweat osmolality in some of the congenital diseases.

Sweat osmolality pattern was studied in Indian sub population of both controls and patients with congenital diseases. A Normal range for sweat osmolality was established for different age groups and sex (100-150 mmols/kg) and compared with the patients, who were clinically diagnosed as cystic fibrosis, Down's syndrome and mentally retarded cases. The study has revealed that sweat osmolality varies according to age and sex in normal population implying the effect of endocrinological changes associated with the onset of puberty. Further, it was also observed that an elevated sweat osmolality is not unique to cystic fibrosis alone, but seen among the Down's syndrome and some of the mentally retarded cases where in the etiology is traced to the inborn errors of metabolism.