This a very complex question - generally, a Trisomy child will manifest the following: hypotonia and hyper-reflexibility of the joints; mental deficiency; microcephaly with a small nasal bridge and inner epicanthal folds; small, overfolding of the ears; short neck; short metacarpals of the hand; anomaly of the heart; loose folds in the posterior neck; fine, soft hair, small penis (eewww) and gonadal deficiency.
#21
Disorders, such as Down's Syndrome, are caused by nondisjunction.
Yes, Non-disjunction occurs when sex chromosomes fail to separate. This occurrence leads to variable numbers of chromosomes and the manifestation of developmental diseases such as Down syndrome, Turner syndrome, etc.
Turner's Syndrome is typically not inherited, as it is caused by a random error in the formation of the egg or sperm. It is often due to a missing or incomplete X chromosome in females. This error occurs sporadically and is not passed down from parents to their children.
Having a sibling with Down syndrome does not directly increase the chances of giving birth to a child with Down syndrome. The risk is influenced by maternal age, not family history. If both parents are carriers of the genetic translocation for Down syndrome, the risk may be higher.
The lungs.
chromosome 21
No age group is affected; Down syndrome is a chromosome condition that is with you at birth.
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Chromosome 21 is tripled in Down syndrome.
It Could Do.
The proportion of men to women with Down syndrome is about equal.
#21
there are approxmately 1/4 million families in the united states affected by down syndrome.
There is no medical treatment that can cure Down syndrome. The best way to treat someone with Down syndrome is with kindness, patience, and love.
Forty-seven. In Down syndrome, there is an extra 21st chromosome. It is also known as Trisomy 21.
It is acceptable to say that someone has Down Syndrome, although it may not be necessary to say it since the syndrome does have a characteristic affect on facial features which can be observed.