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Waardenburg syndrome Waardenburg sendromu
2005Waardenburg Syndrome (WS) is an autosomal dominant syndrome characterized with hearing loss and pigmentation disorders. Its frequency has been reported to be 1/20.000-40.000. Among its clinical features dystopia canthorum, high broad nasal root, synorphrys, heterochromia iridium or isochromic blue irides of both eyes, white forelock, pigmentary ...
Zafer, Cansu, Silan, FATMA
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Yan ke xue bao = Eye science, 1993
We report a patient with Waardenburg syndrome. He suffers from congenital deafness and presents high broad nasal root, synophrys, iris heterochromia and fundus hypopigment. The dystopia canthus is absence. In his family pedigree analysis, we found that his second cousin has oculocutaneous albinism.
D, Li, Q, Ma, Y, Chen, L, Zeng
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We report a patient with Waardenburg syndrome. He suffers from congenital deafness and presents high broad nasal root, synophrys, iris heterochromia and fundus hypopigment. The dystopia canthus is absence. In his family pedigree analysis, we found that his second cousin has oculocutaneous albinism.
D, Li, Q, Ma, Y, Chen, L, Zeng
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Waardenburg's memorial lecture: Waardenburg's syndrome
International Ophthalmology, 1982openaire +2 more sources