Gonadal Hormones

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...

PeLiferia

Riva B, Molinari S, Nicolosi ML, Evasi V, Garella V, Di Marco S, Cattoni A

2023/5 — pag. 89-89 — DOI

An adrenocortical adenoma was diagnosed in a 4-year-old boy presenting with high growth rate, pubic hair and frequent penal erection....

La mini-pubertà

Lattuada M, Calia M, Evasi V, Molinari S, Nicolosi ML, Cattoni A

2022/6 — pag. 131-132 — DOI

The case of mini-puberty in a 6-month-old infant born preterm is described. The authors discuss the clinical differences of mini-puberty in term and preterm newborns....

Un eritema nodoso dalle molte cause

Udina C

2021/10 — pag. 318-318 — DOI

The authors described the case of a 16-year-old girl presenting with erythema nodosum in the lower limbs eventually attributable to the birth control pill (ethinylestradiol)....

Interferenti endocrini e salute dei bambini

F. Chiarelli, L. Comegna, S. Franchini

2018/3 — pag. 157-164

Children and adolescents are daily exposed to substances present in nature and to industrial and chemical products that may interfere with their normal endocrine functions over time. For this reason, such exogenous substances able to cause adverse ...

Diarrea acuta: quando la faccenda è seria… non si parla di probiotici Un medico donna, per favore Cannabidiolo nell’epilessia (sindrome di Dravet): ideologia, ignoranza e scienza Siparietto sull’empiema e dintorni Klinefelter, imprinting testosteronico e… casi indimenticabili

2017/6 — pag. 349-350

Dal pubarca a una sindrome genetica:diagnosi di una malattia rara

E. Benelli, N. Giurici, A. Ventura, M. Rabusin

2017/2 — pag. 107-112

The paper reports the case of a 2-year-old child presenting with pubarche, clitoromegaly and seborrhoea. Her past medical history was unremarkable and no other abnormal sign was found at the physical exam. Karyotype was normal 46 XX. Because of the...

Quando pensare alla sindrome di Kallmann

E. Carlin, F. Colonna, G. Tornese, F. Zennaro

2017/2

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...

Una tumefazione del clitoride

V. Graziani, M. Mainetti, F. Currò, S. Dal Bo, P. Ghetti, A. Zucchini, F. Marchetti

2014/2 — pag. 113-115

Un adrenarca fuori dagli schemi

M.C. Pellegrin

2013/1 — pag. 53-56

Pubarca precoce, irsutismo, amenorrea e bassa statura: quale diagnosi?

A. Zucchini, F. Marchetti

2013/1 — pag. 35-38

Non-classical congenital adrenal hyperplasia (NCCAH) is an autosomal recessive disease that appears during childhood with hyperandrogenic symptoms. The article reports a case of NCCAH due to 21-hydroxylase deficiency in a 14-year-old girl with prem...

Dalle curve di crescita alla diagnosi di sindrome adrenogenitale

D. Cimino, V. Giacchi

2012/7 — pag. 463-464

Non-classical congenital adrenal hyperplasia (NC CAH) is an autosomal recessive disease that appears during childhood with hyperandrogenic symptoms (premature pubarche, accelerated growth, advanced bone age, penile enlargement, and hypertrophy of...

Dalle curve di crescita alla diagnosi di sindrome adrenogenitale

D. Cimino, V. Giacchi

2012/7

Non-classical congenital adrenal hyperplasia (NC CAH) is an autosomal recessive disease that appears during childhood with hyperandrogenic symptoms (premature pubarche, accelerated growth, advanced bone age, penile enlargement, and hypertrophy of...

Linee guida sulla diagnosi e il trattamento del bambino con bassa statura idiopatica

F. Chiarelli, R. Salomone

2008/10 — pag. 626-633

ISS is defined auxologically by a height below -2 SDS without findings of disease after a complete evaluation by a pediatric endocrinologist (including bone age X-ray, thyroid function, karyotype for girls, and measurements of IGF-I and stimulated gr...

Gestione della sindrome di Turner in età pediatricae durante la vita adulta

R. Salomone, F. Chiarelli

2008/3 — pag. 157-165

This consensus statement arose from an interdisciplinary meeting of geneticists, paediatricians, cardiologists, internists, behavioural health specialists, and gynaecologists involved in the care of and clinical research on patients with Turner Syn...

Protocollo in caso di sviluppo puberale precoce

a cura di G. Tonini, E. Faleschini, G. Borotto, I. Giuseppin

2004/1

“Spasmi affettivi”: questione di ferro?Anorchia o criptorchidismo?La vaccinazione contro il virus dell’epatite B riduce l’incidenza del carcinoma epatocellulareCampi magnetici e leucemia nel bambino: sembra che non sia veroPET e CROHN (ma non è una favola danese)Nuove possibilità per la diagnosi prenataleI corticosteroidi per via inalatoria aumentano il rischio di cataratta?L’etidronato nella cura dell’osteoporosi da corticosteroidiIl trapianto di sangue del cordone ombelicale nelle malattie ematologiche (sintesi di esperienza italiana)Enteropatia autoimmune: dalla nascita in poiPorpora trombocitopenica idiopatica, immunoglobuline e splenectomia(Fito)estrogeni e soiaNovità per l’AIDS del bambinoPolimorfismo del gene recettore della vitamina D e densità ossea

1997/7 — pag. 417-418