Abstract Background: Constitutional delay of growth and puberty (CDGP) is classifed as the most frequent cause of delayed puberty (DP). Finding out the etiology of DP during frst evaluation may be a challenge. In details, pediatricians often cannot diferentiate CDGP from permanent hypogonadotropic hypogonadism (PHH), with defnitive diagnosis of PHH awaiting lack of puberty by age 18 yr. Neverthless, the ability in providing a precise and tempestive diagnosis has important clinical consequences. Main text: A growth failure in adolescents with CDGP may occur until the onset of puberty; after that the growth rate increases with rapidity. Bone age is typically delayed. CDGP is generally a diagnosis of exclusion. Nevertheless, other causes of DP must be evaluated. A family history including timing of puberty in the mother and in the father as well as physical examination may givee information on the cause of DP. Patients with transient delay in hypothalamicpituitary-gonadal axis maturation due to associated conditions, such as celiac disease, infammatory bowel diseases, kidney insufciency and anorexia nervosa, may experience a functional hypogonadotropic hypogonadism. PHH revealing testosterone or estradiol low serum values and reduced FSH and LH levels may be connected to abnormalities in the central nervous system. So, magnetic resonance imaging is required in order to exclude either morphological alterations or neoplasia. If the adolescent with CDGP meets psychological difculties, treatment is recommended. Conclusion: Even if CDGP is considered a variant of normal growth rather than a disease, short stature and retarded sexual development may led to psychological problems, sometimes associated to a poor academic performance. A prompt and precise diagnosis has an important clinical outcome. Aim of this mini-review is throwing light on management of patients with CDGP, emphasizing the adolescent diagnosis and trying to answer all questions from paediatricians.

Current clinical management of constitutional delay of growth and puberty

Gaudino, Rossella;
2022-01-01

Abstract

Abstract Background: Constitutional delay of growth and puberty (CDGP) is classifed as the most frequent cause of delayed puberty (DP). Finding out the etiology of DP during frst evaluation may be a challenge. In details, pediatricians often cannot diferentiate CDGP from permanent hypogonadotropic hypogonadism (PHH), with defnitive diagnosis of PHH awaiting lack of puberty by age 18 yr. Neverthless, the ability in providing a precise and tempestive diagnosis has important clinical consequences. Main text: A growth failure in adolescents with CDGP may occur until the onset of puberty; after that the growth rate increases with rapidity. Bone age is typically delayed. CDGP is generally a diagnosis of exclusion. Nevertheless, other causes of DP must be evaluated. A family history including timing of puberty in the mother and in the father as well as physical examination may givee information on the cause of DP. Patients with transient delay in hypothalamicpituitary-gonadal axis maturation due to associated conditions, such as celiac disease, infammatory bowel diseases, kidney insufciency and anorexia nervosa, may experience a functional hypogonadotropic hypogonadism. PHH revealing testosterone or estradiol low serum values and reduced FSH and LH levels may be connected to abnormalities in the central nervous system. So, magnetic resonance imaging is required in order to exclude either morphological alterations or neoplasia. If the adolescent with CDGP meets psychological difculties, treatment is recommended. Conclusion: Even if CDGP is considered a variant of normal growth rather than a disease, short stature and retarded sexual development may led to psychological problems, sometimes associated to a poor academic performance. A prompt and precise diagnosis has an important clinical outcome. Aim of this mini-review is throwing light on management of patients with CDGP, emphasizing the adolescent diagnosis and trying to answer all questions from paediatricians.
: Puberty, Delayed puberty, Bone age, Growth, Constitutional delay of growth and puberty, Hypogonadotropic hypogonadism
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/1062378
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