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Results 61 - 70 of 113 for Short ear
  1. Cri-du-chat syndrome 
    ... features, including widely set eyes (hypertelorism), low-set ears, a small jaw, and a rounded face. Some ... is caused by a deletion of the end of the short (p) arm of chromosome 5. This chromosomal change ...
    https://medlineplus.gov/genetics/condition/cri-du-chat-syndrome - Genetics
  2. Renal tubular acidosis with deafness 
    ... hearing loss caused by changes in the inner ear (sensorineural hearing loss) usually begins between childhood and young adulthood, and gradually gets worse. An inner ear abnormality affecting both ears occurs in most people ...
    https://medlineplus.gov/.../renal-tubular-acidosis-with-deafness - Genetics
  3. Otospondylomegaepiphyseal dysplasia 
    ... of the body that this condition affects: the ears (oto-), the bones of the spine (spondylo-), and ... and is present in the nose and external ears. Type XI collagen is also part of the ...
    https://medlineplus.gov/.../otospondylomegaepiphyseal-dysplasia - Genetics
  4. Diastrophic dysplasia 
    ... mouth (a cleft palate). Swelling of the external ears is also common in newborns and can lead to thickened, deformed ears.The signs and symptoms of diastrophic dysplasia are ...
    https://medlineplus.gov/genetics/condition/diastrophic-dysplasia - Genetics
  5. Weissenbacher-Zweymüller syndrome 
    ... and is present in the nose and external ears. Type XI collagen is also part of the inner ear and the nucleus pulposus, which is the center ... body, including the long bones, spine, and inner ears, which impairs bone development and underlies the other ...
    https://medlineplus.gov/.../weissenbacher-zweymuller-syndrome - Genetics
  6. Cleidocranial dysplasia 
    ... hearing loss and are prone to sinus and ear infections. Some young children with this condition are ... is present in the nose, airways, and external ears.The RUNX2 protein is a transcription factor, which ...
    https://medlineplus.gov/genetics/condition/cleidocranial-dysplasia - Genetics
  7. Saethre-Chotzen syndrome 
    ... growth line that goes over the head from ear to ear. Other parts of the skull may be malformed ... with Saethre-Chotzen syndrome also have small, rounded ears.The signs and symptoms of Saethre-Chotzen syndrome ...
    https://medlineplus.gov/genetics/condition/saethre-chotzen-syndrome - Genetics
  8. Kaufman oculocerebrofacial syndrome 
    ... the eyes that point upward (upslanting palpebral fissures). Ear abnormalities include low-set ears with small lobes and growths of skin (skin tags) in front of the ear (preauricular tags). The nose has a narrow bridge, ...
    https://medlineplus.gov/.../kaufman-oculocerebrofacial-syndrome - Genetics
  9. Xia-Gibbs syndrome 
    ... features, such as a broad forehead, low-set ears or ears that stick out, widely spaced eyes (hypertelorism), eye ... Xia-Gibbs syndrome lead to production of abnormally short AHDC1 proteins. The effects of these changes in ...
    https://medlineplus.gov/genetics/condition/xia-gibbs-syndrome - Genetics
  10. Tetrasomy 18p 
    ... that can include unusually shaped and low-set ears, a small mouth, a flat area between the ... tetrasomy 18p can include seizures, vision problems, recurrent ear infections, mild to moderate hearing loss, constipation and ...
    https://medlineplus.gov/genetics/condition/tetrasomy-18p - Genetics
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