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10.1136/bcr-2016-214764

http://scihub22266oqcxt.onion/10.1136/bcr-2016-214764
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C4885340!4885340 !27199441
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suck abstract from ncbi


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pmid27199441
      BMJ+Case+Rep 2016 ; 2016 (ä): ä
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  • Recurrent spontaneous scleral rupture in Marfan s syndrome #MMPMID27199441
  • Turaga K ; Senthil S ; Jalali S
  • BMJ Case Rep 2016[May]; 2016 (ä): ä PMID27199441 show 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.
  • |Adult [MESH]
  • |Autografts [MESH]
  • |Conjunctiva/*transplantation [MESH]
  • |Humans [MESH]
  • |Male [MESH]
  • |Marfan Syndrome/*complications [MESH]
  • |Rupture, Spontaneous [MESH]
  • |Sclera/*transplantation [MESH]
  • |Scleral Diseases/etiology/*therapy [MESH]
  • |Treatment Outcome [MESH]


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