Sj. Doyle et al., EMMETROPISATION, AXIAL LENGTH, AND CORNEAL TOPOGRAPHY IN TEENAGERS WITH DOWNS-SYNDROME, British journal of ophthalmology, 82(7), 1998, pp. 793-796
Aim-To study the refractive status and corneal topography in Down's sy
ndrome. Method-A matched cohort subgroup of 50 individuals with Down's
syndrome in the Manchester area aged 15-22 years was studied by refra
ction, corneal topography, A-scan biometry, slit lamp examination, and
orthoptic examination. Results-(l) A Linear relation was found betwee
n axial length and spherical equivalent refraction. There was no stati
stical relation between keratometry and the axial length. (2) 80% of t
he group had a hyperopic refraction (mean +2.46 D, range +0.5 to +7.5
D); 18% were myopic (mean -2.75 D, range -0.5 to -8.0 D); and 2% were
emmetropic, (within plus or minus 0.5 D of zero). The overall mean sph
erical equivalent refraction was +1.43 (SD 2.86) D. 63% of eyes could
see 6/12 or better and 66% of the individuals had a binocular vision o
f 6/12 or better. (3) Corneal topography was generally of a regular ''
bow tie'' pattern, but there was a high incidence of oblique cylinders
. Mean cylinder strength was 1.14 (1.15) D. (4) The prevalence of over
t keratoconus was 2%. 6% had corneal topography with inferior steepeni
ng which may be a preclinical keratoconic process. Conclusions-In this
cohort of late teenagers with Down's syndrome, emmetropisation has fa
iled to occur in most individuals. In a similar aged group of non-disa
bled individuals one would expect about 83% emmetropic (plus or minus
0.25 D), 13% myopic, and 4% hyperopic. The wide spread of oblique cyli
nders and the small proportion of with the rule astigmatism is probabl
y related to this failure of emmetropisation. The prevalence of 2% ker
atoconus in Down's syndrome compares with that found by other authors
of between 5.5 and 15%. The 6% with inferior steepening on topography
will be followed up over the next few years to see if there is any dev
elopment of clinical keratoconus. Hence we will see if corneal topogra
phy is useful as a screening tool for preclinical keratoconus in this
high risk group.