Cri Du Chat syndrome was first discovered by a Frenchman, a geneticist named Jerome Lejeune in the year 1963. He was also a pro-life pediatrician who helpe in the discovery of the connection between chromosome abnormalities and diseases. He devoted a major part of his career treating children affected by Down's syndrome.
Dr. Jerome Lejeune first described cri du chat syndrome in 1963
It is evident when they are a baby.....
I believe that approximately 1 out of 200,000-500,00 people has cri du chat
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Cri du chat syndrome is a rare disorder which affects persons missing a part of chromosome 5. Some other names are cat cry syndrome, 5P deletion syndrome, and monosomy 5P.
No, People with Cri Du Chat actually live a generally normal life. ~
Cri du chat is caused during meiosis (the production of sex cells, such as the egg or sperm) when chromosome number 5 is not aligned correctly when separating and part of chromosome number 5 is chipped of, lost, and not repaired correctly or at all. then this cell merges with the other sex cell and a baby with cri du chat is formed
Jerome LeJeune in 1963
See cri-du-chat-syndrome-causes-and-symptoms
See cri-du-chat-syndrome-diagnosis
Cri Du Chat syndrome is a rare Genetic disorder. About 10% of the population has Cri Du chat. There is no cure to this disease.
See cri-du-chat-syndrome-treatment
The scientific name for cri du chat is 5p deletion syndrome.
of 2004 there is no cure for cri du chat syndrome. Treatment consists of supportive care and developmental therapy.
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Cri du Chat Syndrome or Chromosome 5p- is a chromosomal condition that results in brain abnormalities.
I believe that approximately 1 out of 200,000-500,00 people has cri du chat
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approximitley 1 in 20,000- 1 in 50,000 get cri du chat a year