Article

Pigmentary glaucoma in a patient with 48, XXYY syndrome: a case report

2023-11-01

Abstract excerpt

<h4>Objective: </h4> We report a case of a patient with 48, XXYY genetic syndrome suffering from a pigmentary glaucoma. Background The 48, XXYY syndrome is a very rare sporadic genetic condition with a variety of clinical signs and symptoms. Similarly to Klinefelter syndrome, the principal symptom is the hypergonadotrophic hypogonadism leading to infertility. Several other common features of this syndrome includi...

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Literature Corpus work: f9073daa-e736-587b-a821-6123dfdd16ce
DOI: 10.21203/rs.3.rs-3463517/v1

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