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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[edit]
Cause[edit]
Diagnosis[edit]
Treatment[edit]
Prognosis[edit]
History[edit]
The 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[edit]
Category: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