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  2. Congenital vertebral anomaly - Wikipedia

    en.wikipedia.org/wiki/Congenital_vertebral_anomaly

    Lumbarization is an anomaly in the spine. It is defined by the nonfusion of the first and second segments of the sacrum. The lumbar spine subsequently appears to have six vertebrae or segments, not five. This sixth lumbar vertebra is known as a transitional vertebra. Conversely the sacrum appears to have only four segments instead of its ...

  3. Klippel–Feil syndrome - Wikipedia

    en.wikipedia.org/wiki/Klippel–Feil_syndrome

    The three categories treated for types of spinal cord deficiencies are massive fusion of the cervical spine (Type I), the fusion of 1 or 2 vertebrae (Type II), and the presence of thoracic and lumbar spine anomalies in association with type I or type II Klippel–Feil syndrome (Type III).

  4. Segmentation in the human nervous system - Wikipedia

    en.wikipedia.org/wiki/Segmentation_in_the_human...

    The segmentation pattern observed in the spinal nerves is in fact governed by the somatic mesoderm. In the embryonic stages of higher vertebrates including humans, the segmentation of these spinal nerves follows the directions from both the anterior (A, cranial) and posterior (P, caudal) sections of the somite mesoderm.

  5. Scoliosis - Wikipedia

    en.wikipedia.org/wiki/Scoliosis

    Congenital scoliosis can be attributed to a malformation of the spine during weeks three to six in utero due to a failure of formation, a failure of segmentation, or a combination of stimuli. [47] Incomplete and abnormal segmentation results in an abnormally shaped vertebra, at times fused to a normal vertebra or unilaterally fused vertebrae ...

  6. Spina bifida - Wikipedia

    en.wikipedia.org/wiki/Spina_bifida

    Occulta has no or only mild signs, which may include a hairy patch, dimple, dark spot or swelling on the back at the site of the gap in the spine. [5] [1] Meningocele typically causes mild problems, with a sac of fluid present at the gap in the spine. [1] Myelomeningocele, also known as open spina bifida, is the most severe form. [2]

  7. Cervicocranial syndrome - Wikipedia

    en.wikipedia.org/wiki/Cervicocranial_syndrome

    For example GDF6 gene plays an important role in bone development and joint formation. [12] The mutation in these genes can result in Klippel-Feil syndrome . As a result of having congenital Klippel-Feil syndrome , the spinal anatomy of the individual will present abnormal fusion of any two of the seven cervical bones in the neck. [ 13 ]

  8. Ewers vs. Manning: How close is a Texas quarterback ... - AOL

    www.aol.com/sports/ewers-vs-manning-close-texas...

    Ewers’ most visible and glaring flaw is his difficulty throwing downfield, and this is a case where the eye test matches up with the numbers. Over the entire season, Ewers has just seven “Big ...

  9. Neural tube defect - Wikipedia

    en.wikipedia.org/wiki/Neural_tube_defect

    An elevated MSAFP measured at 16–18 weeks gestation is a good predictor of open neural tube defects, however the test has a very high false positive rate, (2% of all women tested in Ontario, Canada between 1993 and 2000 tested positive without having an open neural tube defect, although 5% is the commonly quoted result worldwide) and only a ...