What is Cat Cry Syndrome?

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Cat Cry syndrome, also known as 5P minus or Cri-du-Chat syndrome, is a condition that results in some part of the chromosome missing. This syndrome affects the physical features of the people who were born with it, usually giving them low-set ears and wide-stared eyes. CAT CRY syndrome is also associated with delayed development, low birth weight and low intelligence. Although most cases of this condition are not genetic, it is possible to inherit Cat Cry syndrome. The condition is so -called because affected infants have a cry similar to the condition of the domestic cat. Dislocated hips, split lips and rare kidney conditions are less common symptoms of cat crying syndrome. Due to the influence of the larynx and the nervous system, the cry of an infant or a child is very much like a cat. Some grow up from a characteristic high -resolution shout, although most maintain shouting in Adulthood. Unusual facial features and a small head can become less different because the child reaches adolescence and usually is not visible LaiKem.

This chromosome deletion syndrome is one of the most common affects people. Most often it happens randomly when eggs or sperm form. Cat Cry syndrome is sometimes inherited from one parent who also has a type of chromosome syndrome. Girls are born with a condition a little more often than boys and any ethnicity can be affected. Nevertheless, the condition is not common, although genetic testing can be performed if the future parent fears options.

There is no treatment or specific treatment of Cat Cry syndrome. Various symptoms such as mental retardation or speech problems can be solved. Many affected individuals may never be able to fully function in society or care. However, some are able to understand their primary language well enough to communicate verbally. The severity of Cat Cry syndrome depends strongly on how much and which part of the chromosome is missing.

i kdYZ is CAT CRY syndrome very unusual, many groups and charity organizations have been established around the world. Some organizations maintain a database of members to inform them regularly about meetings and breakthroughs on the syndrome. Caritas usually fund further research or support for families affected by syndrome.

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