Patau syndrome: Difference between revisions

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Patau Syndrome is also known as [https://bms.ncl.ac.uk/wiki/index.php/Trisomy Trisomy] 13 as it is caused my an extra [https://bms.ncl.ac.uk/wiki/index.php/Chromosome chromosome] 13. This is similar to the more well-known [https://bms.ncl.ac.uk/wiki/index.php/Down%27s_syndrome Down's syndrome], except for that, the trisomy occurs on chromosome 21. Patau's is the least common non-lethal trisomies, affectin 1 in 10,000 live-births. Out of this 80% will have a full trisomy, with the remainder having translocation or mosai.cism
Patau Syndrome /ˈpætaʊ/ is also known as [[Trisomy 13|Trisomy 13]] as it is caused by an extra [[Chromosome 13|chromosome 13]]. This is similar to the more well-known [[Down's syndrome|Down's syndrome]], except that the [[Trisomy|trisomy]] occurs on [[chromosome 21|chromosome 21]]. Patau is the least common non-lethal trisomies, affecting 1 in 10,000 live births. Out of this 80% will have a full trisomy, with the remainder having partial trisomy (due to translocation or mosaicism)<ref>http://www.lucinafoundation.org/birthdefects-trisomy13.html</ref><ref>http://www.trisomy.org/resources/soft-publications/trisomy-13-facts/</ref>.  


Symptoms:
There is no treatment for Patau's syndrome.
 
<span style="background-color: initial; font-size: 17.5296px; font-weight: bold;">Symptoms</span>


These can vary greatly, however almost all suffer from severe mental deficiency.  
These can vary greatly, however almost all suffer from severe mental deficiency.  
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*Polydactyly  
*Polydactyly  
*Rocker-bottom feet  
*Rocker-bottom feet  
*Cleft Palate (this occurs in about 60% of those with Patau Syndrome)
*Cleft Palate (this occurs in about 60% of those with Patau Syndrome)  
*Holoprosencephaly (forebrain in the embryo does not divide into two hemispheres)
*Holoprosencephaly (forebrain in the embryo does not divide into two hemispheres)  
*Microcephaly (small head size)
*Microcephaly (small head size)
*Microphthalmia (small eyes)
*Cutis aplasia (skin missing from scalp)
*COngenital heart defect (affects around 80%)
*Ear malformations (can lead to deafness)  
*Microphthalmia (small eyes)  
*Anophthalmia (absence of one or both eyes)
*Hypotelorism (smaller distance between eyes)
*Capillary haemangiomas (raised, red birthmarks)
*Congenital heart defect (affects around 80%)  
*Seizures
 
=== Life expectancy ===
 
Patau syndrome may affect the development of the baby in the womb and can result in miscarriage / stillbirth<ref>https://www.nhs.uk/conditions/pataus-syndrome/</ref>.


<br>  
45% of those born with Patau Syndrome die with one month and 70% within the first 6<ref>http://emedicine.medscape.com/article/947706-overview</ref>, while 90% die within their first year. The median survival age for the patient is about 2.5 days in the United States<ref>http://syndrome.org/patau-syndrome/</ref>.


<br>
About 5-10% of babies with partial or mosaic Patau Syndrome can live for over a year.


<references />http://emedicine.medscape.com/article/947706-overview
=== References ===


<references />http://www.trisomy.org/resources/soft-publications/trisomy-13-facts/
<references />

Latest revision as of 20:33, 11 December 2017

Patau Syndrome /ˈpætaʊ/ is also known as Trisomy 13 as it is caused by an extra chromosome 13. This is similar to the more well-known Down's syndrome, except that the trisomy occurs on chromosome 21. Patau is the least common non-lethal trisomies, affecting 1 in 10,000 live births. Out of this 80% will have a full trisomy, with the remainder having partial trisomy (due to translocation or mosaicism)[1][2].

There is no treatment for Patau's syndrome.

Symptoms

These can vary greatly, however almost all suffer from severe mental deficiency.

Physical:

  • Polydactyly
  • Rocker-bottom feet
  • Cleft Palate (this occurs in about 60% of those with Patau Syndrome)
  • Holoprosencephaly (forebrain in the embryo does not divide into two hemispheres)
  • Microcephaly (small head size)
  • Cutis aplasia (skin missing from scalp)
  • Ear malformations (can lead to deafness)
  • Microphthalmia (small eyes)
  • Anophthalmia (absence of one or both eyes)
  • Hypotelorism (smaller distance between eyes)
  • Capillary haemangiomas (raised, red birthmarks)
  • Congenital heart defect (affects around 80%)
  • Seizures

Life expectancy

Patau syndrome may affect the development of the baby in the womb and can result in miscarriage / stillbirth[3].

45% of those born with Patau Syndrome die with one month and 70% within the first 6[4], while 90% die within their first year. The median survival age for the patient is about 2.5 days in the United States[5].

About 5-10% of babies with partial or mosaic Patau Syndrome can live for over a year.

References