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Brushfield spots are a characteristic feature of the chromosomal disorder Down syndrome or trisomy 21. They occur in 35–78% of newborn infants with Down syndrome. [2] Brushfield spots tend to be obscured by pigmentation of the anterior border layer of the iris in patients with darker irides.
Down syndrome or Down's syndrome, [12] also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. [3] It is usually associated with developmental delays, mild to moderate intellectual disability , and characteristic physical features.
The average IQ of a young adult with Down syndrome is 50, equivalent to the mental age of an 8- or 9-year-old child, but this number varies widely. [3] At the same time, they enjoy a rich social and emotional awareness. [4] Down syndrome is the most common chromosome abnormality in humans, [3] occurring in about one per 1000 babies born each ...
Down Syndrome Risk Factors Advanced maternal age is thought to be the greatest risk factor for Down syndrome, as a mother's eggs, when older, have more chance of chromosomal abnormalities.
A woman's age is a key factor in whether or not her child as at risk for Down syndrome, according to the National Down Syndrome Society. While the chances are 1 in 1,200 for a woman who gets ...
Mom fights for boy with Down syndrome to be included in ad campaign after he's overlooked Mom captures moment 2-month-old says 'hello' on video Baby's Harry Potter photo shoot is the most ...
Sometimes there is a third bigger fontanelle other than posterior and anterior ones in a newborn. In one study, the frequency of third fontanelles in an unselected population of newborn infants was 6.3%. It is very common in Down syndrome and some congenital infections. If present, the physician should rule out serious conditions associated ...
Cat eye syndrome; Caudal regression syndrome; Sotos syndrome Cerebral Gigantism; CHARGE syndrome; Chromosome 16 abnormalities; Chromosome 18 abnormalities; Chromosome 20 abnormalities; Chromosome 22 abnormalities; Cleft lip/palate; Cleidocranial dysostosis; Club foot; Congenital adrenal hyperplasia (CAH) Congenital central hypoventilation syndrome