Physicians and parents alike are under increasing pressure to identify and
to treat short stature, but intervention implies the presence of some patho
logy, physical or psychological, that can be corrected. Where there is true
GH deficiency, the argument for replacement is uncontroversial. It is less
compelling where GH 'insufficiency' is diagnosed. In the case of the short
, but otherwise normal, child the indications for therapy are even less cle
ar. Short stature, per se, is clearly not a disease, in spite of the percep
tion by some practitioners that the rate of growth of such children is abno
rmal. Short stature is, however, commonly perceived to be associated with s
ocial and psychological disadvantage, yet many of these misperceptions abou
t short stature can be challenged. A critical review of the literature pert
aining to the psychosocial correlates of short stature uncovers much flawed
evidence. Most importantly, the belief, widely held by paediatricians, tha
t short children are likely to be significantly disadvantaged, has been fou
nded largely on data from clinic-referred samples. In such studies, childre
n with real (or perceived) behavioural or academic problems are likely to b
e overly represented. Publications arising from such studies, however, inev
itably lead to an increase in the demand for treatment both from and for th
ose who previously had no such concern. In contrast, data from a well contr
olled, prospective population-based study suggest the essential normality o
f the short normal child. Parents and children alike should be reassured by
these findings. In the absence of clear pathology, physical or psychologic
al, GH therapy for short but otherwise normal children must therefore, in m
ost cases, be deemed cosmetic, raising issues as to the ethics of so-called
"plastic endocrinology".