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Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
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| Waardenburg's Syndrome | Legal notice |
Other terms
Syndrome, Waardenburg's,Waardenburg Syndrome,Waardenburgs Syndrome,Klein's Syndrome,Klein Syndrome,Kleins Syndrome,Syndrome, Klein's,Klein-Waardenburg Syndrome,Klein Waardenburg Syndrome,Syndrome, Klein-Waardenburg,Waardenburg-Klein Syndrome,Syndrome, Waardenburg-Klein,Waardenburg Klein Syndrome
Description
Waardenburg's Syndrome: Rare, autosomal dominant disease with variable penetrance and several known clinical types. Characteristics may include depigmentation of the hair and skin, congenital deafness, heterochromia iridis, medial eyebrow hyperplasia, hypertrophy of the nasal root, and especially dystopia canthorum. The underlying cause may be defective development of the neural crest (neurocristopathy). Waardenburg's syndrome may be closely related to piebaldism. Klein-Waardenburg Syndrome refers to a disorder that also includes upper limb abnormalities.
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Legal notice
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The version of the data is 2010 MeSH. Last reviewed April 26, 2010. No modification has been made in the content of the file.
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