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- Discovered first in 1916 by a Dutch ophthalmologist, it went through many studies over the years, finally being named and formulated by Petrus Johannes Waardenburg in 1951. He broke the disorder into four categories. Type 2A is the type that ferrets are most often afflicted with.
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Apr 6, 2023 · What Is Waardenburg Syndrome? Discovered first in 1916 by a Dutch ophthalmologist, it went through many studies over the years, finally being named and formulated by Petrus Johannes Waardenburg in 1951. He broke the disorder into four categories. Type 2A is the type that ferrets are most often afflicted with.
Jul 10, 2015 · Anecdodally, it has been suggested that 75% of US ferrets with a blaze or white head can suffer from the Waardenburg syndrome and are deaf (J. Mayer, personal observation).
- Joerg Mayer, Robert P. Marini, James G. Fox
- Laboratory Animal Medicine. 2015 : 577-622.
- 10.1016/B978-0-12-409527-4.00014-6
- 2015
This article will explain everything you need to know about Waardenburg syndrome, which is also called Neural Crest disorder in ferrets. We’ll discuss how to tell if your ferret is affected by the condition and look at common symptoms and ways that you can test your ferret to see if it’s deaf.
Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye ), a white forelock or patches of light skin.
Mar 21, 2022 · Waardenburg syndrome causes minor defects of the neural crest pathways of affected ferrets, and is related to certain colour and pattern combinations of the fur, which often indicate the presence of the condition.
Mar 30, 2024 · This article will cover everything you need to know about Waardenburg syndrome in ferrets, commonly known as Neural Crest disease. We’ll look at typical signs and techniques to test your ferret to see whether it’s deaf, as well as how to detect if your ferret has the condition.
Waardenburg syndrome presents within the population in four main types that are categorized by either their phenotypic or genotypic characteristics. Most often, the syndrome displays an autosomal dominant pattern of inheritance.
