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  2. Patau syndrome - Wikipedia

    en.wikipedia.org/wiki/Patau_syndrome

    Trisomy 13 is the cause of Patau syndrome, which means each cell in the body has three copies of chromosome 13 instead of the usual two. A small percentage of cases occur when only some of the body's cells have an extra copy; such cases are called mosaic trisomy 13. [citation needed]

  3. Confined placental mosaicism - Wikipedia

    en.wikipedia.org/wiki/Confined_placental_mosaicism

    The common autosomal trisomies (21, 18, 13) made up a smaller number of cases of mosaicism detected on CVS, but were more often confirmed in fetal tissue (19%). [3] On the other hand, the uncommon autosomal trisomies accounted for a greater number of placental mosaicism cases, but were less often confirmed in fetal tissue (3.2%). [ 3 ]

  4. Chromosome 13 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_13

    Trisomy 13: Trisomy 13 occurs when each cell in the body has three copies of chromosome 13 instead of the usual two copies. Trisomy 13 can also result from an extra copy of chromosome 13 in only some of the body's cells (mosaic trisomy 13). In a small percentage of cases, trisomy 13 is caused by a rearrangement of chromosomal material between ...

  5. 13q deletion syndrome - Wikipedia

    en.wikipedia.org/wiki/13q_deletion_syndrome

    13q deletion syndrome is a rare genetic disease caused by the deletion of some or all of the large arm of human chromosome 13. Depending upon the size and location of the deletion on chromosome 13, the physical and mental manifestations will vary. It has the potential to cause intellectual disability and congenital malformations that affect a ...

  6. A mom of 3 learned she had mosaic Down syndrome through ... - AOL

    www.aol.com/lifestyle/mom-3-learned-she-had...

    A mother shares her story about being diagnosed with mosaic Down syndrome. A mom of 3 learned she had mosaic Down syndrome through genetic testing. Here's why she's 'happy' with the diagnosis.

  7. Pallister–Killian syndrome - Wikipedia

    en.wikipedia.org/wiki/Pallister–Killian_syndrome

    Individuals with PKS present prenatally or at birth with multiple birth defects.These defects include: brain atrophy, agenesis of the corpus callosum, polymicrogyria of the brain, and/or spot calcifications in the brain's lateral sulcus; deafness and/or blindness; autonomic nervous system dysfunctions such as anhidrosis, hypohidrosis, and/or episodic spells of hyperventilation interspersed ...

  8. Triploid syndrome - Wikipedia

    en.wikipedia.org/wiki/Triploid_syndrome

    Congenital heart defects, hydronephrosis, omphalocele and meningocele (spina bifida) are also common. Cystic hygromas occur but are uncommon. [citation needed] Triploid fetuses have intrauterine growth restriction beginning early in the pregnancy, as early as 12 weeks, and does not affect the head as severely as the body.

  9. Pregnant Keke Wyatt Reveals Baby No. 11 'Tested Positive for ...

    www.aol.com/entertainment/pregnant-keke-wyatt...

    Keke Wyatt. Mediapunch/Shutterstock Holding onto hope. Pregnant Keke Wyatt revealed that her baby-to-be has been diagnosed with a genetic disorder — and slammed Instagram haters’ responses to ...

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