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  2. Preauricular sinus and cyst - Wikipedia

    en.wikipedia.org/wiki/Preauricular_sinus_and_cyst

    Preauricular sinuses and preauricular cysts are two common congenital malformations. Each involves the external ear. The difference between them is that a cyst does not connect with the skin, but a sinus does. [3] Frequency of preauricular sinus differs depending the population: 0.1–0.9% in the US, 0.9% in the UK, and 4–10% in Asia and ...

  3. Branchial cleft cyst - Wikipedia

    en.wikipedia.org/wiki/Branchial_cleft_cyst

    Treatment. Conservative, surgical excision. A branchial cleft cyst or simply branchial cyst is a cyst as a swelling in the upper part of neck anterior to sternocleidomastoid. It can, but does not necessarily, have an opening to the skin surface, called a fistula. The cause is usually a developmental abnormality arising in the early prenatal ...

  4. Submandibular lymph nodes - Wikipedia

    en.wikipedia.org/wiki/Submandibular_lymph_nodes

    The most common causes of enlargement of the submandibular lymph nodes are infections of the head, neck, ears, eyes, nasal sinuses, pharynx, and scalp. The lymph glands may be affected by metastatic spread of cancers of the oral cavity, anterior portion of the nasal cavity, soft tissues of the mid-face, and submandibular salivary gland.

  5. Why some people have a small hole in front of their upper ears

    www.aol.com/article/lifestyle/2016/11/29/why...

    It is called preauricular sinus which, according to the U.S. National Institutes of Health, or NIH, "generally appears as a tiny skin-lined hole or pit, often just in front of the upper ear where ...

  6. Branchio-oto-renal syndrome - Wikipedia

    en.wikipedia.org/wiki/Branchio-oto-renal_syndrome

    Branchio-oto-renal syndrome. Branchio-oto-renal syndrome has an autosomal dominant pattern of inheritance. Branchio-oto-renal syndrome (BOR) [4] [5] is an autosomal dominant genetic disorder involving the kidneys, ears, and neck. It is also known as Melnick-Fraser syndrome. [2] [3]

  7. Rhinomanometry - Wikipedia

    en.wikipedia.org/wiki/Rhinomanometry

    Rhinomanometry is a standard diagnostic tool aiming to objectively evaluate the respiratory function of the nose. It measures pressure and flow during normal inspiration and expiration through the nose. Increased pressure during respiration is a result of increased resistance to airflow through nasal passages (nasal blockage), while increased ...

  8. Sinus pericranii - Wikipedia

    en.wikipedia.org/wiki/Sinus_pericranii

    Sinus pericranii is a venous anomaly where communication between the intracranial dural sinuses and dilated epicranial venous structures exists. That venous anomaly is a collection of non-muscular venous blood vessels adhering tightly to the skull's outer surface and directly communicating with intracranial venous sinuses through diploic veins ...

  9. Empty nose syndrome - Wikipedia

    en.wikipedia.org/wiki/Empty_nose_syndrome

    Empty nose syndrome ( ENS) is a clinical syndrome, the hallmark symptom of which is a sensation of suffocation despite a clear airway. This syndrome is often referred to as a form of secondary atrophic rhinitis. ENS is a potential complication of nasal turbinate surgery or injury. [1] [2] Patients have usually undergone a turbinectomy (removal ...

  10. Current Procedural Terminology - Wikipedia

    en.wikipedia.org/wiki/Current_Procedural_Terminology

    The Current Procedural Terminology ( CPT) code set is a procedural code set developed by the American Medical Association (AMA). It is maintained by the CPT Editorial Panel. [1] The CPT code set describes medical, surgical, and diagnostic services and is designed to communicate uniform information about medical services and procedures among ...

  11. Ellis–Van Creveld syndrome - Wikipedia

    en.wikipedia.org/wiki/Ellis–van_Creveld_syndrome

    Ellis–Van Creveld syndrome is caused by a mutation in the EVC gene, as well as by a mutation in a nonhomologous gene, EVC2, located close to the EVC gene in a head-to-head configuration. The gene was identified by positional cloning. [4] The EVC gene maps to the chromosome 4 short arm (4p16). The function of a healthy EVC gene is not well ...