Spontaneous lens resorption in a patient with Marshall-Stickler Syndrome and glaucoma

患有马歇尔-斯蒂克勒综合征和青光眼的患者发生自发性晶状体吸收

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Abstract

PURPOSE: The purpose of this case report is to describe the increased fragility of anterior capsule in patients with the rare genetic disease Marshall-Stickler syndrome. OBSERVATIONS: We describe a 3-year old patient with Marshall-Stickler Syndrome and congenital glaucoma treated with glaucoma drainage implant placement who subsequently developed spontaneous lens resorption in one eye, which was noted incidentally during one follow-up appointment. CONCLUSIONS AND IMPORTANCE: It is hypothesized that the lens material left the eye through the glaucoma drainage implant over time. This process was not associated with elevation of intraocular pressures or inflammation and did not require subsequent surgery to remove any residual lens fragments, which has not been reported before to the best of the authors' knowledge.

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