Data concerning final height (FH) in isolated growth hormone deficiency typ
e 1A (IGHD1A) are scanty and controversial. In this paper we report the FH
outcome of two girls with IGHD1A who were treated either with GH only (firs
t patient) or with GH during the first 8 years and successively with IGF-I
(second patient). In the first patient, FH was only slightly subnormal and
slightly taller with respect to target height (TH). Surprisingly, FH was se
verely subnormal and very far from TH in the patient who underwent IGF-I th
erapy for >5 years: an auxological outcome similar to the one recently repo
rted in the only two cases in the literature of patients with IGHD1A who ha
ve been treated with IGF-I until near FH achievement, We conclude that IGHD
1A could have a very heterogeneous phenotypic expression in terms of FH and
that IGF-I therapy, even though initiated some years before puberty onset
and prolonged for more than 5 years, may not be able to ensure the normaliz
ation of height prognosis and the achievement of an FH close to TH.