The development of secondary sexual characteristics in adolescents is a sign of normal physiological development (
3,
5). Therefore, evaluating the onset and progression of the early signs of sexual development and sexual maturation are important in the assessment of individual health. In addition, with the knowledge of normal puberty age, we can define precocious or late puberty (
5).
The age for the onset of puberty and secondary sexual characteristics, as well as factors affecting this process, have been discussed in different regions of the world. It has been proven that pubertal onset varies across different populations (
5,
12). In addition, nutritional status, economic conditions, and disease have a significant impact on the timing of puberty events (
13).
In Iran, several studies have been conducted to investigate the age of puberty onset among healthy children and adolescents (
4,
5,
14). In a study on 7,493 healthy Iranian girls, Rabbani et al. (
4) found that the mean ages for the start of maturity based on the B2 and P2 stages of maturity according to the Tanner classification were 10.1 and 9.38 years, respectively. In the present study which included 643 female students with intellectual, sensory, or physical disabilities from Tehran the average age for the onset of puberty was 10.8 years based on reaching the B2 stage and 10.79 years based on reaching the P2 stage. These findings show a slight delay in puberty compared to the age reported by Rabbani et al. (
4) for the healthy population.
Razzaghy et al. (
5) have reported the mean age of the onset of puberty for healthy Iranian girls to be 9.74 years based on B2 and 10.49 years based on P2. According to their findings, our patients demonstrate delayed puberty onset compared to the healthy population (
4). Similar to our findings, in 1975, Salerno et al. showed that females with intellectual disability show a delay in puberty compared to healthy individuals (
15). A similar delay has been reported by Evans et al. (
16) in mentally handicapped females.
The delay in puberty in this group of children might be related to eating disorders or the side effects of some medications such as corticosteroids and psychotropic drugs as well as a higher incidence of endocrine diseases (
17-
19). As a general rule in mental and motor disabilities with genetic and chromosomal origin, impaired development of the neuroendocrine system and the evolution of the GnRH-producing neurons causes a delay of gonadal development, which can cause a delay of puberty (
20).
Cento et al. (
9) have reported that FSH secretion in response to GnRH treatment in the early stages of puberty was impaired in females with intellectual disability. They concluded that the low sensitivity of cells secreting FSH may be due to dysfunction of catecholaminergic, opioid, or GABAergic routes
In this study, children in different age groups were shorter compared to the healthy peers reported on by Rabbani et al. (
4) The average height in the Rabbani et al. study was reported to be 140.3 cm in the B2 stage, but it was only 128.2 cm among our participants. Previous studies on patients with intellectual disability in Tehran indicate similar findings (
21). This is similar to a finding of Baidwan et al. (
17) on patients with intellectual disability from India (
10). Although eating disorders can be considered as the cause of this finding, associated endocrine disorders such as GH-IGF1 axis dysfunction, thyroid disorders, and other unknown conditions should be considered. This explains the fact that in the Baidwan et al. study, despite the elimination of eating disorders as a factor, short stature was still present. In 2009, Kuperminc et al. (
17) studied 20 six to 18-year-old patients with cerebral palsy for three years and compared them to a group of 63 healthy children in terms of growth before and during puberty. Children with cerebral palsy were behind in all stages of their growth compared to healthy controls. This study indicated a defect in the GH-IGF1 axis among patients.
The present study had some shortcomings. For example, due to a lack of access to the medical records of children, we could not divide our participants based on the type of underlying disease (cerebral palsy, Down syndrome, etc.); therefore, the cause of intellectual disability was not identified. In addition, we had no control group in this study, which might limit the reliability of our results.
5.1. Conclusion
In our patients, the mean ages of onset of puberty indicated by breast budding (B2 stage) and by pubic hair growth (P2 stage) were 10.8 ± 1.48 years and 10.79 ± 1.64 years, respectively. Compared to the data from healthy Iranian girls, our findings indicate that the mean age of pubertal onset in schoolgirls with disabilities is slightly higher than that of their healthy counterparts.