Waardenburg syndrome 2 with ocular albinism
Waardenburg syndrome 2 with ocular albinismAn autosomal dominant disorder (OMIM:103470) characterised by ocular albinism with sensorineural deafness.
Caused by defects of MITF, which encodes microphthalmia-associated transcription factor, a protein that regulates differentiation and development of melanocytes and retinal pigment epithelium, and is responsible for pigment cell-specific transcription of melanogenesis enzyme genes.
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