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  2. Saethre–Chotzen syndrome - Wikipedia

    en.wikipedia.org/wiki/Saethre–Chotzen_syndrome

    Saethre–Chotzen syndrome (SCS), also known as acrocephalosyndactyly type III, is a rare congenital disorder associated with craniosynostosis (premature closure of one or more of the sutures between the bones of the skull).

  3. Cervicocranial syndrome - Wikipedia

    en.wikipedia.org/wiki/Cervicocranial_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] This is considered to be an anomaly of cervical bones. [14] It affects the functioning of cervical spinal nerves (C1 - C8) because of compression on the spinal cord.

  4. Noonan syndrome - Wikipedia

    en.wikipedia.org/wiki/Noonan_syndrome

    Facial features include widely spaced eyes, light-colored eyes, low-set ears, a short neck, and a small lower jaw. [1] Heart problems may include pulmonary valve stenosis. [1] The breast bone may either protrude or be sunken, while the spine may be abnormally curved. [1] Intelligence is often normal. [1] Complications of NS can include leukemia ...

  5. Bone age - Wikipedia

    en.wikipedia.org/wiki/Bone_age

    A child's current height and bone age can be used to predict adult height. [4] Other uses of bone age measurements include assisting in the diagnosis of medical conditions affecting children, such as constitutional growth delay, precocious puberty, thyroid dysfunction, growth hormone deficiency, and other causes of abnormally short or tall stature.

  6. Cleidocranial dysostosis - Wikipedia

    en.wikipedia.org/wiki/Cleidocranial_dysostosis

    Cleidocranial dysostosis (CCD), also called cleidocranial dysplasia, is a birth defect that mostly affects the bones and teeth. [1] The collarbones are typically either poorly developed or absent, which allows the shoulders to be brought close together. [1]

  7. Treacher Collins syndrome - Wikipedia

    en.wikipedia.org/wiki/Treacher_Collins_syndrome

    In children, an autologous bone graft is mostly used. In combination with this transplantation, lipofilling can be used in the periorbital area to get an optimal result of the reconstruction. [ citation needed ] Reconstruction of the lower eyelid coloboma includes the use of a myocutaneous flap, which is elevated and in this manner closes the ...

  8. Doctor claims screens are damaging children's eyes - AOL

    www.aol.com/doctor-claims-screens-damaging...

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  9. Craniosynostosis - Wikipedia

    en.wikipedia.org/wiki/Craniosynostosis

    The supraorbital bar is the rim just above the eye socket; as discussed under phenotype, the supraorbital and the frontal bone are typically recessed at the ipsilateral side of the head. [54] The goal of treatment is to position this bar together with the frontal bone in a plane three millimetres further forwards than the vertical plane of the ...