Difference between revisions of "Trisomy 21"

Jump to navigation Jump to search

Trisomy 21 (view source)

Revision as of 03:35, 5 May 2012

1,017 bytes removed ,  03:35, 5 May 2012
mv to 'down syndomre'
(mv to 'down syndomre')
 
(4 intermediate revisions by the same user not shown)
Line 1: Line 1:
'''Trisomy 21''', also known as '''Down syndrome''', is a common genetic abnormality.
#redirect [[Down syndrome]]
 
==Characteristics==
Mnemonic ''CHILD HAS PROBLEM'':<ref>URL: [http://www.valuemd.com/genetics.php http://www.valuemd.com/genetics.php]. Accessed on: 29 May 2011.</ref>
*[[congenital heart disease|'''C'''ongenital heart disease]] / Cataracts.
*Hypotonia / Hypothyroidism.
*Incurved 5th finger / Increased gap between 1st and 2nd toe.
*[[Leukemia]] risk x2 / Lung problem.
*Duodenal atresia / Delayed development.
*[[Hirschsprung disease]] / Hearing loss.
*[[Alzheimer disease]] / Alantoaxial instability.
*Squint / Short neck.
*Protruding tongue/ Palmar crease.
*Round face / Rolling eye (nystagmus).
*Occiput flat / Oblique eye fissure.
*Brushfield spot / Brachycephaly.
*Low nasal bridge / Language problems.
*Epicanthic fold / Ears folded.
*Mental retardation / Myoclonus.
 
==See also==
*[[Trisomy 13]] (Patau syndrome).
*[[Trisomy 18]] (Edwards syndrome).
*[[Chromosomal anomalies]].
*[[Stillbirth]].
 
==References==
{{Reflist|1}}
 
[[Category:Syndromes]]
Michael
48,470

edits

Retrieved from "https://librepathology.org/wiki/Special:MobileDiff/5695...16074"

Navigation menu