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10.1136/bcr-2016-214764 http://scihub22266oqcxt.onion/10.1136/bcr-2016-214764 C4885340!4885340!27199441     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       BMJ+Case+Rep 2016 ; 2016 (ä): ä Nephropedia Template TP {{tp|p=27199441|t=2016. Recurrent spontaneous scleral rupture in Marfan s syndrome |pdf=|usr=}}{{27199441}} gab.com Text Recurrent spontaneous scleral rupture in Marfan s syndrome JO: BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=27199441 #FOAvip The ocular manifestations of Marfan's syndrome (MS) range from ectopia lentis, microspherophakia, myopia, glaucoma and retinal detachment. Spontaneous scleral rupture is a rare complication and recurrent scleral perforation is extremely rare. We report a rare case of a 26-year-old male with MS who had sequential recurrent spontaneous scleral rupture which required surgical repair. He suffered from a similar problem 4?years later in both eyes in a different location, with overlying thin cystic blebs and hypotony maculopathy. Surgical repair with preserved scleral donor patch graft and conjunctival autograft in one eye, and conjunctival advancement in the other eye was performed. This helped stabilise the eyes, and resulted in complete visual recovery in both eyes. Twit Text FOAVip Recurrent spontaneous scleral rupture in Marfan s syndrome ????BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=27199441 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27199441 #FOAvip English Wikipedia <ref>{{Cite pmid|27199441}}</ref> Recurrent spontaneous scleral rupture in Marfan s syndrome #MMPMID27199441 Turaga K; Senthil S; Jalali S BMJ Case Rep 2016[]; 2016 (ä): ä PMID27199441show ga The ocular manifestations of Marfan's syndrome (MS) range from ectopia lentis, microspherophakia, myopia, glaucoma and retinal detachment. Spontaneous scleral rupture is a rare complication and recurrent scleral perforation is extremely rare. We report a rare case of a 26-year-old male with MS who had sequential recurrent spontaneous scleral rupture which required surgical repair. He suffered from a similar problem 4?years later in both eyes in a different location, with overlying thin cystic blebs and hypotony maculopathy. Surgical repair with preserved scleral donor patch graft and conjunctival autograft in one eye, and conjunctival advancement in the other eye was performed. This helped stabilise the eyes, and resulted in complete visual recovery in both eyes. äRecurrent spontaneous scleral rupture in Marfan s syndrome (epmc).pdf DeepDyve Pubget Overpricing