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Trisomy 13


Trisomy 13 is also known as Patau syndrome and occurs when the child receives duplicated information from chromosome #13. This disorder affects approximately 1 in every 10,000 babies.

Common symptoms of the disorder include cleft palate/cleft lip, close set or fused eyes (becoming a cyclops), low muscle tone, polydactyly, hernia, coloboma, severe mental retardation, undescended testicles in the male, small eyes and head, seizures, missing skin, skeletal malformations and low set ears.

Babies will generally have feeding complications, breathing abnormalities, heart complications and will be deaf. Because of the severe malformations of the disorder, most affected babies are either stillborn or die within the first few months of life.





Comments: Trisomy-13

Comments 1 to 2 of about 2.


LuckyNo.3 - 90 days ago.
My little angel was born almost 3 weeks ago and that is when we found out he had Trisomy 13. He was with us for 9 wonderful days when God called for him. It was the most difficult thing I have had to go through and feel for anyone who has lost a loved one. I still struggle everyday and at times wonder WHY but I know that God had a plan for him and I am at peace that he is not suffering anymore. He made my family stronger and will never be forgotten!!

allyson - 112 days ago.
I had twin boys who were fraternal on July 3, 2008. Sadly, one of my boys was diagnosed with T-13. He lived for 21 days, and I miss him terribly. I declined the amnio, so the only clue I had that there might be something wrong with him was at the 13 week scan. The doctor told me that he had a SUA- single umbilical artery. We put our trust in God, and he blessed us with a beautiful little boy. We enjoyed him every moment of his life, and I will never forget him.


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Forum & Info: Birth defects & disorders

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  • 1A1V-(Single-Umbilical-Artery) 12
  • Achondrogenesis-Syndrome 0
  • Achondroplasia 0
  • Allan-Herndon-Dudley-Syndrome 0
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  • Cleidocranial-Dysplasia 1
  • Clubfoot 12
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  • Congenital-Heart-Defect 12
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  • Hydrocele 0
  • Hydrocephalus 2
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  • Hypospadias 8
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  • Iniencephaly 0
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  • Jervell-and-Lange-Nielsen-Syndrome 0
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  • Joubert-Syndrome 1
  • Juberg-Marsidi-Syndrome 0
  • Kasabach-Merritt-Syndrome 0
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  • Klippel-Trenaunay-Syndrome 0
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  • Labial-Fusion 0
  • Laurence-Moon-Syndrome 0
  • LEOPARD-Syndrome 0
  • Leri-Weil-Syndrome 1
  • Lissencephaly 0
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  • McCune-Albright-Syndrome 0
  • McKusick-Kaufman-Syndrome 0
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  • Miller-Syndrome 0
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  • Muenke-Syndrome 0
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  • Myelomeningocele 0
  • Nager-Syndrome 0
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  • Neuronal-Migration-Disorder 0
  • Noonan-Syndrome 0
  • Norrie-Disease 0
  • Ollier`s-Disease 1
  • Omphalocele 1
  • Opitz-G-BBB-Syndrome 0
  • Osteogenesis-Imperfecta 0
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  • Penile-Agenesis 0
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  • Phenylketonuria-(PKU) 0
  • Pierre-Robin-Sequence 0
  • Platyspondylic-Lethal-Skeletal-Dysplasia 0
  • Poland-Syndrome 0
  • Polydactyly 0
  • Polymicrogyria 0
  • Porencephaly 0
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  • Posterior-Urethral-Valves 1
  • Prader-Willi-Syndrome 0
  • Progeria 0
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  • Renal-Agenesis 4
  • Rett-Syndrome 1
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  • Stork-Bites 9
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  • Tay-Sachs-Disease 0
  • test 2
  • Tethered-Spinal-Cord-Syndrome 1
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  • Trisomy-18 3
  • Trisomy-21 7 (1 new)
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