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  2. Microtia - Wikipedia

    en.wikipedia.org/wiki/Microtia

    Microtia is a congenital deformity where the auricle (external ear) is underdeveloped. A completely undeveloped auricle is referred to as anotia. Because microtia and anotia have the same origin, it can be referred to as microtia-anotia. [1] Microtia can be unilateral (one side only) or bilateral (affecting both sides).

  3. Low-set ears - Wikipedia

    en.wikipedia.org/wiki/Low-set_ears

    Low-set ears are a clinical feature in which the ears are positioned lower on the head than usual. They are present in many congenital conditions. Low-set ears are defined as the outer ears being positioned two or more standard deviations lower than the population average. [1] Clinically, if the point at which the helix (curved upper part) of ...

  4. Ear - Wikipedia

    en.wikipedia.org/wiki/Ear

    An ear is the organ that enables hearing and (in mammals) body balance using the vestibular system. In mammals, the ear is usually described as having three parts: the outer ear, the middle ear and the inner ear. The outer ear consists of the pinna and the ear canal. Since the outer ear is the only visible portion of the ear in most animals ...

  5. Noonan syndrome - Wikipedia

    en.wikipedia.org/wiki/Noonan_syndrome

    Noonan syndrome ( NS) is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems, and skeletal malformations. [1] Facial features include widely spaced eyes, light-colored eyes, low-set ears, a short neck, and a small lower jaw. [1]

  6. Anotia - Wikipedia

    en.wikipedia.org/wiki/Anotia

    Anotia ("no ear") describes a rare congenital deformity that involves the complete absence of the auricle, the outer projected portion of the ear, and narrowing or absence of the ear canal. This contrasts with microtia, in which a small part of the auricle is present. Anotia and microtia may occur unilaterally (only one ear affected) or ...

  7. 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 ). This affects the shape of the head and face, resulting in a cone-shaped head and an asymmetrical face.

  8. Orangutan - Wikipedia

    en.wikipedia.org/wiki/Orangutan

    Orangutans have small ears and noses; the ears are unlobed. The mean endocranial volume is 397 cm 3. The cranium is elevated relative to the face, which is incurved and prognathous. Compared to chimpanzees and gorillas, the brow ridge of an orangutan is underdeveloped.

  9. Pointy ears - Wikipedia

    en.wikipedia.org/wiki/Pointy_ears

    The pointed ear (s) in Stahl's ear is caused by misshapen cartilage. It is characterized by an extra horizontal fold of cartilage (crus). Normally, there are two: superior and inferior. In Stahl's ear, there is a third horizontal crus. The helix (or upper portion of the ear) may uncurl, giving the ear a pointed shape.