Waardenburg Syndrome: A Case Report
Sara Sadiq, Azizullah Langah, Ali Akbar Siyal & Noor Ul Ain Ali · Asian Journal of Pediatric Research · 2019
Waardenburg syndrome is an uncommon autosomal dominant or recessive disorder, distinguished by hypopigmentation of either skin or hairs or both, segmental, partial or complete heterochromia iridis or isohypochromia, hypertrichosis of eyebrow, synophrys, dystopia canthorum, broad...
Open access
Research Article
10.9734/ajpr/2019/v2i430113