Abstract: Primary ciliary dyskinesia (PCD) is a rare hereditary disease; it can rarely coexist with other rare disorders such as retinitis pigmentosa which is a hereditary cause of blindness by retinal ciliary dysfunction. This association is not obvious at first sight. We report the case of a patient with retinitis pigmentosa and bronchiectasis as the first apparent symptom of PCD.
KEY WORDS: primary ciliary dyskinesia, bronchiectasis, retinitis pigmentosa
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