A piebald person can be perfectly normal whereas Waardenburg syndrome is a group of genetic conditions that can cause hearing loss and hypopigmentation of the hair, skin, and eyes.
Waardenburg syndrome is typically inherited in an autosomal dominant pattern, meaning that only one copy of the mutated gene is needed to develop the condition. However, there are rare cases where it can be inherited in an autosomal recessive pattern, requiring two copies of the mutated gene.
There are thousands of different types of disorders that impact the mind and body. These can range from mental health disorders like anxiety and depression to physical illnesses such as diabetes and heart disease. Each disorder has its own set of symptoms, causes, and treatments.
Nondisjunction can lead to abnormal chromosome numbers in daughter cells, resulting in conditions such as Down syndrome, Turner syndrome, or Klinefelter syndrome. This can cause developmental issues, intellectual disabilities, and various physical abnormalities in affected individuals.
It is a congenital condition, marked by facial and craniological differences. There are also Internet references made to "Harry Benjamin Syndrome," the cause, some say, of Transgender and Gay people. However, there is not any scientific documentation that this is in any way a causal factor.
Individuals with Down syndrome often exhibit abnormal brain wave patterns compared to typical individuals, including a higher incidence of epileptiform activity. They may also show differences in frequency and amplitude of brain waves during cognitive tasks. These differences may be related to structural abnormalities in the brain associated with Down syndrome.
If you are referring to Poliosis (decrease or absence of melanin in hair of the head) there are a number of diseases associated with it, here are a few: Waardenburg Syndrome - associated with deafness Piebaldism - associated with abnormal skin pigmentation Partial Albinism - associated with eye problems Vogt-Koyanagi-Harada Syndrome - associated with eye problems http://en.wikipedia.org/wiki/Poliosis http://en.wikipedia.org/wiki/Waardenburg%27s_syndrome http://en.wikipedia.org/wiki/Piebaldism http://en.wikipedia.org/wiki/Albinism http://en.wikipedia.org/wiki/Vogt-Koyanagi-Harada
Pietrus sp? Waardenburg discovered Waardenburg syndrome in the Netherlands. It was the early 50s. I think it was 1951. He was a Dutch ophthmologist (eye doctor MD) who discovered many school children with different colored eyes (heterochromatica ) were deaf. WS is a leading cause of deafness.
Waardenburg syndrome affects people of all ethnicities equally. However, certain features of the syndrome may be more noticeable in individuals with lighter skin and hair due to the contrast in pigmentation.
Waardenburg synrome is an autosomal genetic disorder characterized by deafness, confluent brows, early grey hair as young as 12, different colored eyes or unusually brilliant blue eyes. Source US NIH Deafness and other communcation disorders. Its named Waardenburg because it was discovered Prietrus Waardenburg who noticed girls and boys with unmatching eyes tend to deafness. There are four main types.
Glaucoma, Waardenburg syndrome, Neurofibromatosis, or some mild infection infecting one eye.
Waardenburg syndrome is a genetic condition characterized by hearing loss and pigmentation differences, while dyspraxia is a developmental coordination disorder affecting physical coordination and movement. There is no established direct link between the two; however, some individuals with Waardenburg syndrome may experience challenges that could overlap with dyspraxia, particularly in motor skills or coordination. Further research is needed to explore any potential connections or shared underlying factors.
# Meningitis # Prebycusis # Otis Media # Tinnitus # Pematurity # Cytomegaloirus # treacher collinssyndrome # Waardenburg syndrome
The population of Waardenburg is 2,330.
Waardenburg syndrome is typically inherited in an autosomal dominant pattern, meaning that only one copy of the mutated gene is needed to develop the condition. However, there are rare cases where it can be inherited in an autosomal recessive pattern, requiring two copies of the mutated gene.
I think the only way Waardenburg syndrome would be deadly is indirect. That is if one is deaf because of it If one crosses the street and doesn't the traffic going that would the way WS is deadly. In other words if because of deafness one is less conscience of possible dangers in one's life. The physical symptoms such as different colored eyes, eyebrows that tend to come together, premature gray haii is far from dangerous.
Approximately 5% of cleft conditions are associated with a genetic syndrome, including Van der Woude, Opitz, Aarskog, Fryns, Waardenburg, and Coffin-Siris.
Petrus Johannes Waardenburg was born in 1886.