Wernicke's encephalopathy and Korsakoff syndrome are believed to be two stages of the same condition.
Wernicke's encephalopathy is caused by damaging changes in the brain, usually due to a lack of vitamin B1 (thiamine).
A lack of vitamin B1 is common in people with Alcoholism. Heavy alcohol use affects the breakdown of thiamine in the body. Even if someone who drinks alcohol heavily follows a well-balanced diet, most of the thiamine is not absorbed.
Korsakoff syndrome, or Korsakoff psychosis, tends to develop as Wernicke's symptoms go away. Korsakoff psychosis involves damage to areas of the brain involved with memory.
The Koro syndrome is a culture-specific syndrome. The individual with Koro syndrome has an overpowering belief that his or her genitals are retracting and disappearing.
Down syndrome
You may be thinking of the Dorothy Lack syndrome which many people call the White Coat Syndrome.
is William syndrome caused by a mutation
Restless Leg Syndrome (RLS) is also known in the medical community as Ekbom Syndrome and Wittmaack-Ekbom Syndrome. Anxietas Tiblarum and Anxietas Tibialis are also medical names for Restless Leg Syndrome.
Syndactyly is a characteristic of Apert syndrome, Poland syndrome, Jarcho-Levin syndrome, oral-facial-digital syndrome, Pfeiffer syndrome, and Edwards syndrome
Stockholm syndrome.
The Koro syndrome is a culture-specific syndrome. The individual with Koro syndrome has an overpowering belief that his or her genitals are retracting and disappearing.
Syndactyly is a characteristic of Apert syndrome, Poland syndrome, Jarcho-Levin syndrome, oral-facial-digital syndrome, Pfeiffer syndrome, and Edwards syndrome.
XXXY Syndrome and Barr-Shaver-Carr Syndrome are the same.
Cushing's Syndrome
Disorders, such as Down's Syndrome, are caused by nondisjunction.
yes there is.
what is kinefelter syndrome?
Angelman syndrome is a genetic disorder, as is Down syndrome. But they are not the same. Angelman Syndrome involves a deletion of Chromosome 15, whereas people with Down syndrome have an extra copy of Chromosome 21.
also known as Martin-Bell syndrome, Marker X syndrome, and FRAXA syndrome
no