icrotia varies
from the complete absence of auricular tissues
(anotia) to a somewhat normal but small ear with a narrowed canal. Between
these extremes, one finds an endless variety of vestiges, the most common
being a vertically-oriented sausage-shaped nubbin (see Fig 5). As noted
from the statistical summary of my 1,000 microtia patients (see Table 1),
microtia is nearly twice as frequent in males as in females, and the right-left-bilateral ratio
is roughly 6:3:1.
Figure 5 - Variance of the microtia deformity.
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Grade I, II, III microtia, and anotia (complete absence of any ear remnant). |
Grade l |
Grade ll |
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|
Grade lll |
Anotia |
In most instances, the microtic lobule is displaced superiorly to the level of the opposite, normal side; although incomplete ear migration during development occasionally leaves it in an inferior location. Approximately one-third of the patients exhibit gross characteristics of hemifacial microsomia, although Converse and associates [33, 34] have demonstrated with X-ray studies that bony deficiencies exist in all cases. Whatever the deformity, I have been impressed with its potential for psychological havoc amongst the entire family, varying from the patient's emotional insecurity to the parents' deep-seated guilt feelings (even though it's not their fault).



