Does anyone know almost treacher-kellogg's syndrome ?
Answers: Ok, first stale, it is called Treacher Collins Syndrome.
Treacher Collins syndrome is a condition that affects the nouns of bones and other tissues in the obverse. The signs and symptoms of this disorder vary greatly, range from almost unnoticeable to severe. Most affected individuals enjoy underdeveloped facial bones, remarkably the cheek bones, and a very small jowl and chin (micrognathia). Some people beside this condition are also born with an pipe in the roof of the mouth call a cleft palate. In severe cases, underdevelopment of the facial bones may restrict an affected infant's airway, cause potentially life-threatening respiratory problems.
People with Treacher Collins syndrome recurrently have eyes that slant downward, sparse eyelashes, and a hollow out in the lower eyelids call a coloboma. Some affected individuals own additional eye abnormality that can lead to nightmare loss. This condition is also characterized by absent, small, or unusually formed ears. Defects within the middle ear (which contains three small bones that transmit sound) cause audible range loss in roughly speaking half of cases. People beside Treacher Collins syndrome usually have commonplace intelligence.
Treacher Collins Syndrome is believed to be caused by a make over in the gene on chromosome 5, which affects facial nouns. About 40 percent of the time, one parent has the Treacher Collins Syndrome gene. Geneticists can very soon determine whether the Treacher Collins gene is a new mutation or one that have been passed on. Unless you or your partner own the gene, your medication won't cause it.
More Questions and Answers ...