Difference between revisions of "Trisomy 13"

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==Features==
==Features==
*Midface abnormality - key feature.
*Midface abnormality - '''key feature'''.
**An extreme example: holoprosencephaly - failure of the forebrain to divide into hemispheres.<ref>URL: [http://dictionary.reference.com/browse/Holoprosencephaly http://dictionary.reference.com/browse/Holoprosencephaly]. Accessed on: 16 May 2011.</ref>
*Cardiac abnormalities.
*Aplasia cutis congenita ([[AKA]] aplasia cutis) - congenital absence of hair; usu. on the scalp.<ref>URL: [http://dictionary.reference.com/browse/Aplasia+cutis+congenita http://dictionary.reference.com/browse/Aplasia+cutis+congenita]. Accessed on: 16 May 2011.</ref>
*Polydactyly - more than the normal number of digits.<ref>URL: [http://dictionary.reference.com/browse/polydactyl http://dictionary.reference.com/browse/polydactyl]. Accessed on: 16 May 2011.</ref>
*Horseshoe kidney.
 
==See also==
*[[Stillbirth]].
 
==References==
{{Reflist|2}}


[[Category:Syndromes]]
[[Category:Syndromes]]

Revision as of 14:54, 16 May 2011

Trisomy 13, also known as Patau syndrome, is a relatively common chromosomal abnormality.

Features

  • Midface abnormality - key feature.
    • An extreme example: holoprosencephaly - failure of the forebrain to divide into hemispheres.[1]
  • Cardiac abnormalities.
  • Aplasia cutis congenita (AKA aplasia cutis) - congenital absence of hair; usu. on the scalp.[2]
  • Polydactyly - more than the normal number of digits.[3]
  • Horseshoe kidney.

See also

References