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  2. Nuchal scan - Wikipedia

    en.wikipedia.org/wiki/Nuchal_scan

    How to define a normal or abnormal nuchal translucency measurement can be difficult. The use of a single millimeter cutoff (such as 2.5 or 3.0 mm) is inappropriate because nuchal translucency measurements normally increases with gestational age (by approximately 15% to 20% per gestational week from 10 to 13 weeks). [10]

  3. Obstetric ultrasonography - Wikipedia

    en.wikipedia.org/wiki/Obstetric_ultrasonography

    Perhaps the most common such test uses a measurement of the nuchal translucency thickness ("NT-test", or "Nuchal Scan"). Although 91% of fetuses affected by Down syndrome exhibit this defect, 5% of fetuses flagged by the test do not have Down syndrome. Ultrasound may also detect fetal organ anomaly.

  4. External occipital protuberance - Wikipedia

    en.wikipedia.org/wiki/External_occipital...

    The inion is the most prominent projection of the protuberance which is located at the posterioinferior (rear lower) part of the human skull. The nuchal ligament and trapezius muscle attach to it. The inion (ἰνίον, iníon, Greek for the occipital bone) is used as a landmark in the 10-20 system in electroencephalography (EEG) recording.

  5. Nuchal ligament - Wikipedia

    en.wikipedia.org/wiki/Nuchal_ligament

    From the anterior border of the nuchal ligament, a fibrous lamina is given off. This is attached to the posterior tubercle of the atlas, and to the spinous processes of the cervical vertebrae, and forms a septum between the muscles on either side of the neck. The trapezius and splenius capitis muscle attach to the nuchal ligament.

  6. File:Nuchal translucency Dr. Wolfgang Moroder.jpg - Wikipedia

    en.wikipedia.org/wiki/File:Nuchal_translucency...

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  8. The cast of “Friends” is well known for being besties, but that developed over time. During an appearance on Dax Shepard’s “Armchair Expert” podcast, “Friends” star Lisa Kudrow ...

  9. 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 ...