Coexistence of bilateral macular edema and pale optic disc in the patient with Cohen syndrome
Cohen syndrome (Q87.8;ORPHA:193; OMIM#216550) is an autosomal recessive inherited genetic disorder caused by mutation in the VPS13B/COH1 gene. It is characterized by variable clinical symptoms such as deformity of the head, face, hands and feet, eye abnormalities, abdominal obesity, neutropenia and...
Main Authors: | , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
De Gruyter
2021-01-01
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Series: | Open Medicine |
Subjects: | |
Online Access: | https://doi.org/10.1515/med-2021-0208 |