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  2. Harlequin-type ichthyosis - Wikipedia

    en.wikipedia.org/wiki/Harlequin-type_ichthyosis

    Visible plates on the skin and changes in the appearance of the ears and fingers, are symptoms of Harlequin-type ichthyosis. [10] Newborns with harlequin-type ichthyosis present with thick, fissured armor-plate hyperkeratosis. [11] Sufferers feature severe cranial and facial deformities. The ears may be very poorly developed or absent, as may ...

  3. Protruding ear - Wikipedia

    en.wikipedia.org/wiki/Protruding_ear

    Boy with otapostasis. Father and son with otapostasis. Protruding ear, otapostasis or bat ear is an abnormally prominent human ear. It may be unilateral or bilateral. The concha is large with poorly developed antihelix and scapha. It is the result of malformation of cartilage during primitive ear development in intrauterine life. [1]

  4. Noonan syndrome - Wikipedia

    en.wikipedia.org/wiki/Noonan_syndrome

    The development of the ears and auditory system may be affected in people with Noonan's syndrome. This can result in low-set ears (in over 90%), backward-rotated ears (over 90%), thick helix (outer rim) of ear (over 90%), incomplete folding of ears, chronic otitis media (ear infections), and hearing loss.

  5. CHARGE syndrome - Wikipedia

    en.wikipedia.org/wiki/CHARGE_syndrome

    CHARGE syndrome (formerly known as CHARGE association) is a rare syndrome caused by a genetic disorder.First described in 1979, the acronym "CHARGE" came into use for newborn children with the congenital features of coloboma of the eye, heart defects, atresia of the nasal choanae, restricted growth or development, genital or urinary abnormalities, and ear abnormalities and deafness. [1]

  6. Low-set ears - Wikipedia

    en.wikipedia.org/wiki/Low-set_ears

    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 the outer ear meets the cranium is at or below the line connecting the inner canthi of eyes (the bicanthal plane), the ears are considered low set ...

  7. Fryns syndrome - Wikipedia

    en.wikipedia.org/wiki/Fryns_syndrome

    In a newborn boy thought to have Fryns syndrome, Clark and Fenner-Gonzales (1989) found mosaicism for a tandem duplication of 1q24-q31.2. [3] They suggested that the gene for this disorder is located in that region.

  8. Hearing Aids With Earmolds Vs. Rubber Domes: What to Know

    www.aol.com/lifestyle/hearing-aids-earmolds-vs...

    Universal pieces made to fit a range of ear sizes. Can easily be replaced. Allow more natural hearing. Dome tips are generic pieces that help your hearing aid attach to your ear.

  9. Carpenter syndrome - Wikipedia

    en.wikipedia.org/wiki/Carpenter_syndrome

    A baby affected by Carpenter syndrome will also display malformations of the face. An individual affected by the syndrome may have broad cheeks, a flat nasal bridge, and a wide upturned nose with abnormally large nasal openings. Their ears will most commonly be low, unevenly set, and malformed in structure.