M. Ludwig et al., THE EMBRYONIC-DEVELOPMENT OF SENSORY ORGANS AND THE SKULL IN THE TRISOMY-16 MOUSE, AN ANIMAL-MODEL FOR DOWNS-SYNDROME, ANNALS OF ANATOMY-ANATOMISCHER ANZEIGER, 179(6), 1997, pp. 525-533
The trisomy 16 mouse is a widely accepted animal model for the study o
f the embryonic development of human trisomy 21. While the development
of the brain and heart has been thoroughly studied, there are hardly
any data on the development of sensory organs like the eye, nose and e
ar. By studying scanning electron microscopic pictures and semithin se
ctions from the tenth to the 15th day of development, we found delayed
development of the nose, and, in particular, of the vomer. Sensory st
ructures of the otic vesicle also showed a marked developmental delay.
Pigmentation of the outer layer of the otic cup starts later in triso
mic animals. Cleared specimens on day 16 showed retarded development o
f ossification centres in all areas of the skull. These findings corre
spond with the abnormal facial morphology found in Down's syndrome and
may also provide new insights into the hearing impairment commonly fo
und. The observations in the eye and skull bones indicate that neural
crest tissue maldevelopment is not the sole cause of malformations.