it is a large genatalia wart that only some men grow on the tip of there penis
it is a large genatalia wart that only some men grow on the tip of there penis
Waardenburg syndrome is a genetic disorder effecting hair, eye, facial pigment. It can effect facial features too such a shape of lips, nose bridge, eyebrows. It is most definitely not a genitalia , genital wart.
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.
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.
Piebaldism and Waardenburg syndrome are both genetic disorders that affect pigmentation. However, piebaldism primarily causes a white forelock or patch of white hair and depigmented skin areas, while Waardenburg syndrome is characterized by wider-ranging symptoms including deafness, changes in skin pigmentation, and abnormalities of the eyes, hair, or face shape. Waardenburg syndrome is generally more variable and can affect multiple systems beyond just pigmentation.
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.
The disorder is autosomal dominant, so she would have gotten the gene from either one of her parents. Since not every person has the same symptoms, and symptoms can be very subtle, it's possible for one of her parents to carry the gene without knowing it. Some people with the syndrome have only minor signs, like a patch of white hair, without any difficulties related to hearing or the muscular system. Consulting with a genetic counselor may be helpful for your family as you sort out this question. Best wishes! Waardenburg syndrome can skip a generation or as above the signs can so subtle as to be unrecognizable. I read of a case where a woman gave birth to triplets with Waardenburg when there was no known instances of the genetic syndrome
Glaucoma, Waardenburg syndrome, Neurofibromatosis, or some mild infection infecting one eye.
# 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.
No.
No, Down's syndrome is only a human genetic disorder. Those with the disorder have an extra chromosome. Raccoons do not get this particular genetic disorder.