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.
Some organizations that support individuals with Cri-du-Chat syndrome include the National Organization for Rare Disorders (NORD), the Cri du Chat Syndrome Support Group, and Unique (Rare Chromosome Disorder Support Group). These organizations provide information, resources, and support for individuals with Cri-du-Chat syndrome and their families.
Cri du chat syndrome is a genetic condition caused by a deletion of genetic material on chromosome 5. While it can lead to intellectual disability and developmental delays, the syndrome itself is not considered fatal, and individuals with Cri du chat syndrome can live into adulthood with appropriate medical care and support.
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.
I believe that approximately 1 out of 200,000-500,00 people has cri du chat
Cri Du Chat syndrome is caused by a deletion of genetic material on the short arm of chromosome 5. This deletion occurs randomly and is not inherited from parents. It disrupts normal development and results in the characteristic features of the syndrome.
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.
Some organizations that support individuals with Cri-du-Chat syndrome include the National Organization for Rare Disorders (NORD), the Cri du Chat Syndrome Support Group, and Unique (Rare Chromosome Disorder Support Group). These organizations provide information, resources, and support for individuals with Cri-du-Chat syndrome and their families.
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approximitley 1 in 20,000- 1 in 50,000 get cri du chat a year