521 research outputs found

    Caprellids (Crustacea: Amphipoda) from India

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    The caprellid fauna of India is investigated. A total of 538 samples (including algae, seagrasses, sponges, hydroids, ascidians, bryozoans, encrusted dead corals, coral rubble, fine and coarse sediments) were collected from 39 stations along the coast of India, covering a wide diversity of habitats from intertidal to 12 m water depth. A new species (Jigurru longimanus n.sp.) is described, and figures of the 11 valid species reported so far from India are given together with a key for their identification. No caprellids were found in sediments from the northeast (16–208N) coast of India while they were abundant in the southeast and west coast. Decreases in salinity due to river discharges associated with lower values of oxygen, higher water temperatures and lower nutrient inputs along the east coast could explain these differences in caprellid composition between the two coastlines. Significantly, lower abundance of caprellids in India, as in other tropical ecosystems, is probably related to the lack of species belonging to the genus Caprella, which reach very high abundances in temperate waters.Ministerio de Educación y Ciencia de España y fondos FEDER de la Unión Europea. CGL2007-60044/ BOSConsejería de Innovación, Ciencia y Empresa, Junta de Andalucía, España. P07-RNM-02524Ministry of Earth Sciences (MoES) de India. DOD/10-MLR/1/2002/DT 19.12.200

    Flip-flop jet nozzle extended to supersonic flows

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/76991/1/AIAA-11725-757.pd

    Angle-closure glaucoma

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    In India primary angle closure disease comprises approximately fifty percent of primary glaucoma. It is the leading cause of blindness from glaucoma. Appropriate identification and institution of therapy can prevent long term morbidity from this disease. The use of Pilocarpine and the application of laser iridotomy early in the treatment of angle closure glaucoma has to be underscored. Long term prognosis depends upon identification of the variety of presentations and appropriate use of medical and laser and surgical therapy to maintain a good quality of life for the patients. Family screening plays an important role in detecting new patients at an early stage of the disease

    Aurolab aqueous drainage implant: My surgical technique

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    Aurolab aqueous drainage implant is a nonvalved tube implant used to treat refractory glaucoma. Although implanting the device could be surgically more demanding than certain other drainage devices, the author aims to describe the techniques which enable him to perform the surgery safely and efficiently

    Trabeculectomy with scleral patch graft for advanced glaucoma in ehler–danlos syndrome

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    We report a case of secondary glaucoma in Ehler–Danlos syndrome (EDS) Type VI, which was uncontrolled with maximal medical therapy, and was subsequently managed surgically. EDS comprises a subgroup of heritable connective tissue disorders characterized by generalized joint hypermobility, skin hyperextensibility, and tissue fragility. The surgical challenges in these patients are presence of scleral thinning, vascular fragility, and poor wound healing. Surgical intervention such as trabeculectomy in EDS has not been reported in the literature. With this case report, we share our trials and tribulations in managing this patient with trabeculectomy without antimetabolites, with unexpected modification in the surgery and success

    Mefenamic acid-induced bilateral transient myopia, secondary angle closure glaucoma and choroidal detachment

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    Drug-induced secondary angle closure is quite common and in the majority of cases simply stopping the medication leads to rapid reversal of the condition and resolution of glaucoma. We describe here a patient who presented with secondary angle closure glaucoma and myopia following mefenamic acid ingestion which was managed successfully by stopping the medication, symptomatic treatment and reassurance

    Comparison between ocular biometry parameters in patients with unilateral congenital glaucoma

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    Purpose: To compare the axial length (AL) and corneal diameter between glaucomatous eye (GE) and fellow normal eye (NE) in patients with unilateral congenital glaucoma and to obtain a normative database for ocular growth among Indian children below 3 years of age. Methods: Retrospective longitudinal study. Patients who had a follow-up of 3 years from diagnosis with ocular biometry parameters being recorded at least thrice (once a year) and fellow eye being normal were included. Data collected were age, gender, intraocular pressure (IOP), AL, corneal diameter, optic disc findings, diagnosis, and surgery details. Results: Eleven patients were analyzed. All GE underwent combined trabeculotomy with trabeculectomy. Mean (SD) baseline IOP, AL, and corneal diameter were 17.1 (6.7) mmHg, 18.9 (1.1) mm and 12 (0.91) mm in GE, and 11.1 (3.8) mmHg, 17.8 (0.44) mm, and 10.5 (0.58) mm in NE, respectively. Increase in AL was 3.1 mm in the first year followed by 0.6 mm in second year and 0.4 mm in third year in GE compared to 2.6, 0.6, and 0.5 mm in NE, respectively. Corneal diameter increased by 1.1 mm in GE in the first year and remained stable thereafter compared to 0.7 mm in first year followed by 0.3 mm in second year and stable thereafter in NE. The percentage of success was 73% at 3 years. Conclusion: Axial length and corneal diameter were higher in GE than NE at all-time points. With prompt intervention, the growth curve of the GE was made parallel to that of NE

    Bilateral idiopathic spontaneous filtering bleb with ectopia lentis: A case report and review of literature

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    A 26-year-old male presented with superior filtering bleb with scleral thinning, dislocated lens, and hypotony in both the eyes. His cornea was normal without any sign of ectasia, and there was no history of recurrent redness, trauma, or surgery in either eye. Anterior segment optical coherence tomography did not reveal communicating fistula between the anterior chamber and subconjunctival space. Physical examination and blood investigations did not reveal any systemic association. He was diagnosed to have spontaneous filtering bleb, which is a rare condition observed with ocular or systemic abnormalities
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