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Cri-du-Chat Syndrome...medical consulting

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In this page talks about ( Cri-du-Chat Syndrome...medical consulting ) It was sent to us on 05/08/2021 and was presented on 05/08/2021 and the last update on this page on 05/08/2021

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Symptoms of Cri-du-Chat Syndrome











Symptoms of cri-du-chat syndrome often include a characteristic high-pitched mewing cry that sounds like a kitten crying. This cry may be heard immediately after birth lasts several weeks and then disappears. However not all affected newborns have this distinct cry. An infant with this syndrome may have a low birth weight and a small head with many abnormal features including a round face small jaw wide nose widely separated eyes crossed eyes (strabismus) and abnormally shaped ears set low in the head. Often the infant seems limp. Webbed fingers and toes (syndactyly) and heart defects are common. There are significant limitations in mental and physical development. Many children with cri du chat syndrome survive to adulthood but have substantial disabilities.


Treatment of Cri-du-Chat Syndrome













Supportive care






Treatment of cri-cu-chat syndrome is supportive.


Diagnosis of Cri-du-Chat Syndrome













Chromosomal testing






The diagnosis of cri-du-chat syndrome may be suspected before birth or by the child's physical characteristics after birth. The diagnosis can be confirmed by chromosomal testing.


simple explanation



Cri-du-chat syndrome is a chromosomal deletion syndrome in which part of chromosome 5 is missing.


(See also Overview of Chromosome Disorders.)


Cri-du-chat syndrome is a rare syndrome in which part of chromosome 5 is missing. The size of the missing part varies and people who have larger deletions are often more severely affected.


Symptoms of cri-du-chat syndrome often include a characteristic high-pitched mewing cry that sounds like a kitten crying. This cry may be heard immediately after birth lasts several weeks and then disappears. However not all affected newborns have this distinct cry. An infant with this syndrome may have a low birth weight and a small head with many abnormal features including a round face small jaw wide nose widely separated eyes crossed eyes (strabismus) and abnormally shaped ears set low in the head. Often the infant seems limp. Webbed fingers and toes (syndactyly) and heart defects are common. There are significant limitations in mental and physical development. Many children with cri du chat syndrome survive to adulthood but have substantial disabilities.


Chromosomal testing


The diagnosis of cri-du-chat syndrome may be suspected before birth or by the child's physical characteristics after birth. The diagnosis can be confirmed by chromosomal testing.


Supportive care


Treatment of cri-cu-chat syndrome is supportive.
  • The Author: wikbe
 
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