ipogonadismo

Bassa statura non sindromica e ritardo puberale: non solo ritardo costituzionale di crescita e pubertà

Campanile C, Improda N, Incoronato S, Ferrara A, Gentile G, Colantuoni M, Mandato C, Licenziati MR.

2024/9 — pag. 597-600 — DOI

A 14-year-old boy with suspected constitutional delay of growth and puberty (CDGP) presented with short stature, absence of secondary sex characteristics, bone age delayed by one year and family history of CDGP in his mother. The external genitalia w...

Bassa statura non sindromica e ritardo puberale: non solo ritardo costituzionale di crescita e pubertà

Campanile C, Improda N, Incoronato S, Ferrara A, Gentile G, Colantuoni M, Mandato C, Licenziati MR

2024/9 — pag. 171-174 — DOI

A 14-year-old boy with suspected constitutional delay of growth and puberty (CDGP) presented with short stature, absence of secondary sex characteristics, bone age delayed by one year and family history of CDGP in his mother. The external genitalia w...

La sindrome di Klinefelter

Cattoni A, Nicolosi ML, Tarani L, Selicorni A.

2024/3 — pag. 181-183 — DOI

L’adolescente obeso: è importante valutare i genitali

B. Mainetti, M.T. Nasi, E. Valletta

2018/9 — pag. 595-596

The article describes the case of an adolescent male with obesity and pubertal delay whose hormonal and imaging investigations led to the diagnosis of prolactin secreting pituitary adenoma. After cabergoline treatment, a decrease in prolactinoma size...

Ipogonadismi, terapia ormonale sostitutiva dello sviluppo puberale

G. Tornese, E. Conversano

2015/7

Sindrome di klinefelter:che cosa deve sapere il pediatra?

R. Cavallo, C. Santelia, G. Tornese

2015/2 — pag. 104-110

Klinefelter syndrome (KS), characterized by the presence of at least one extra X chromosome, is the most common chromosomal abnormality in males. Nevertheless, it is highly underdiagnosed (only 25% of expected diagnoses) or is diagnosed later in li...

Non sempre l’appetito è indice di “benessere”

C. Cubaiu, G. Masia

2013/7

Guida pratica per il bambino con sindrome di Prader-Willi

G. Tornese, S. Pastore, G. Tonini

2012/3 — pag. 195-196

Although Prader-Willi syndrome is a rare disease, it provides an excellent example of how early diagnosis and meticulous management can significantly improve long-term prognosis of some genetic diseases. These guidelines, particularly addressed t...

Guida pratica per il bambino con sindrome di Prader-Willi

G. Tornese, S. Pastore, G. Tonini

2012/3

Although Prader-Willi syndrome is a rare disease, it provides an excellent example of how early diagnosis and meticulous management can significantly improve long-term prognosis of some genetic diseases. These guidelines, particularly addressed to fa...