Based on the search results, there is no recognized medical condition officially named "Waldorf disease." However, the term appears in a few different, distinct contexts:

What is the Waldorf syndrome?

Description. Collapse Section. Waardenburg syndrome is a group of genetic conditions that can cause hearing loss and changes in coloring (pigmentation) of the hair, skin, and eyes. Although most people with Waardenburg syndrome have normal hearing, moderate to profound hearing loss can occur in one or both ears.

What celebrities have Waardenburg syndrome?

Although Waardenburg syndrome is rare, it has affected a few notable individuals. One such individual is the film and television actress Mila Kunis, who has heterochromia, a common feature of Waardenburg syndrome, with one brown eye and one green eye. Her condition has contributed to her unique and striking appearance.

What ethnicity has Waardenburg syndrome?

WORLDWIDE DISTRIBUTION OFWAARDENBURG SYNDROME

A computerized literature review found sporadic cases of the syndrome in many ethnic groups, including Japanese, Taiwanese, and Middle Eastern families. The highest reported incidence is among Kenyan Africans.

What are the facial features of Waardenburg syndrome?

Characteristic morphologic features of Waardenburg syndrome can be recognized immediately or soon after birth. Features typically include white forelock, broad nasal root, and hypopigmented irides. Parents notice that the child does not react to sounds.

Waldorf School Education

Which parent passes on Gilbert syndrome?

Risk factors for Gilbert syndrome include: Both parents carry the modified gene that causes the disorder.

What is the attitude of someone with Williams syndrome?

Individuals with William syndrome are often described as hyper-sociable, talkative and friendly, often very empathetic, polite, and happy. People with WS may also display behavior issues and anxiety beginning at a very young age, and some may have specific phobias and fears.

Who is the oldest progeria survivor?

The oldest known person with progeria (Hutchinson-Gilford syndrome) was Sammy Basso from Italy, who passed away in October 2024 at age 28, while Tiffany Wedekind of Ohio (in her mid-40s as of late 2024/early 2025) is a prominent, long-lived individual with a similar rapid-aging condition and is sometimes cited as the oldest, though Sammy holds the record for classic progeria, with advancements extending life expectancy beyond the typical 14 years.
 

Is Waardenburg syndrome autism?

Waardenburg syndrome can be associated with autism spectrum disorder. Regular developmental surveillance is needed for children with Waardenburg syndrome, alongside monitoring of vision and hearing.

What is Miley Cyrus's heart condition?

She was born with supraventricular tachycardia, a condition causing an abnormal resting heart rate. Her birth name, Destiny Hope, expressed her parents' belief that she would accomplish great things. Her parents nicknamed her "Smiley", which they later shortened to "Miley", because she often smiled as an infant.

Does Angelina Jolie have central heterochromia?

Angelina Jolie has central heterochromia, where many colors radiate out from the central pupil. Kate Bosworth has sectoral heterochromia, like my daughter.

What is another name for Waardenburg syndrome?

Also known as Shah–Waardenburg syndrome, or Waardenburg–Shah syndrome, type 4 has most of the same features as type 2 (i.e. no telecanthus, or apparent wider eye gap), but with the addition of Hirschsprung's disease, which is a congenital lack of nerves in the intestines leading to bowel dysfunction.

What is the Waldorf way of life?

In the world of Waldorf, everything comes down to this exact spirit of connection, in every season and in every part of a child's life. As Rudolf Steiner describes, "Life as a whole is a unity, and we must not only consider the child, but the whole of life; we must look at the whole human being."

What genetic disorder causes white hair?

Piebaldism is an autosomal dominant disorder of melanocyte migration and development characterized by isolated congenital leukoderma (white skin) and poliosis (white hair) in a distinct ventral midline pattern.

What is the brutal disease that accelerates aging?

Progeria (pro-JEER-e-uh), also known as Hutchinson-Gilford progeria syndrome, is an extremely rare, progressive genetic disorder. It causes children to age rapidly, starting in their first two years of life. Children with progeria generally appear healthy at birth.

Who's the oldest person living right now in 2025?

Ethel Caterham, recognized by Guinness World Records as the oldest person living, turns 116 on Aug. 21, 2025.

Are there twins with progeria?

A pair of male monozygotic twins, both affected by progeria is described. The concordance in this manifestation suggests a genetic aetiology and other evidence indicates the implication of autosomal recessive factors; the chromosomes of these patients show no detectable abnormalities.

What famous person has Williams syndrome?

While there aren't many widely known celebrities with Williams Syndrome (WS), prominent individuals include Canadian actress Gabrielle Marion-Rivard, musician Ben Monkaba, singer Gloria Lenhoff, and public media figure Amy Kotch, alongside advocate and documentary subject Cali Truelove, all known for their talents and distinctive sociable personalities.

What race is Williams syndrome most common in?

According to the Williams Syndrome Association, WS affects one in 7,500 – 10,000 people worldwide, including an estimated 20,000 to 30,000 people in the United States. It occurs equally in males and females and every race and ethnicity.

Can you take Tylenol if you have Gilbert's syndrome?

The finding suggested that the usual therapeutic dose of acetaminophen is safe for the GS patient. The combination of mutation analysis in UGT1A1 and acetaminophen loading test may be useful to avoid adverse effect in GS patients.

How do you feel when your bilirubin is high?

If it builds up in your blood, it can make you feel ill. It can also irritate nerves under your skin, making it itch. What are symptoms of high bilirubin? High bilirubin leads to jaundice, a yellow cast to your skin and the whites of your eyes.

Is exercise good or bad for Gilbert's?

For people with Gilbert's Syndrome, whose symptoms could be triggered by sudden high intensity exercise, as well as other people who may not be used to exercise – low to moderate intensity exercise is the best place to start.

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