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The maxillary
prominences enlarge considerably to develop the majority of the midface area in the
mature human face (Fig. 2.9) [10].
The distal nasolacrimal lacrimal system is formed by the fusion of the lateral nasal
prominence and the maxillary prominence and starts as a nasolacrimal furrow (Fig. 2.10). As
these two prominences fuse, a double layer of epithelium is trapped between them. At first,
this cord of epithelial cells is in a relatively horizontal orientation as depicted in Fig. 2.10, but
as the maxillary prominences develop and the midface enlarges, this cord of cells assumes a
more mature vertical position (Fig. 2.10). Near birth or soon after, this solid cord of cells
canalizes and forms the nasolacrimal duct [11].
Mandibulofacial dysostosis syndrome, also known as Treacher Collins syndrome, is a good
example of how insults at the embryonic stage can result in craniofacial deformities. This
condition can be induced when a 9-day-old mouse embryo (approximately equal to a 4-
week human embryo) is treated with retinoic acid. This produces a cell deficiency in the
proximal aspect of the maxillary and mandibular prominences (Fig. 2.11). This early
embryonic cell deficiency is manifested in the mature infant as the hypoplastic midface and
jaw area seen in this syndrome [12–14].