Ohdo syndrome, also known as Ohdo blepharophimosis syndrome, is a rare genetic disorder characterised by blepharophimosis (narrow eyelid openings), ptosis (drooping eyelids), dental hypoplasia, hearing impairment and intellectual disability.
Signs and symptoms
editCause
editDiagnosis
editTreatment
editPrognosis
editHistory
editThe syndrome was first identified by Ohdo et al. in 1986.[1]
References
edit- ^ "OMIM Entry - % 249620 - OHDO SYNDROME". omim.org. Retrieved 2021-06-17.
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External links
editCategory:Rare syndromes Category:Syndromes affecting the eyes Category:Syndromes affecting the kidneys Category:Syndromes affecting the gastrointestinal tract Category:Syndromes affecting head size Category:Syndromes affecting the heart