Rivista di formazione e aggiornamento professionale del pediatra e del medico di base, fondata nel 1982. In collaborazione con l'Associazione Culturale Pediatri.
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Adrenal Hyperplasia, Congenital

13 articoli — 2002-2018

RI Percorsi clinici
Il macrorchidismo monolaterale

A. Zucchini, V. Graziani, M. Cozzolino, F. Marchetti

2018/9 — pag. 569-572

The unilateral enlargement of a testis, in the absence of symptoms that point towards an acute scrotum, is a situation that must require careful assessment because the exclusion of a tumour process is the first step to be taken. Tumour or endocrine d...

RI Aggiornamento
Sarà maschio o femmina?

L. Lucaccioni, A. Boncompagni, E. Pietrella, P.L. Ceccarelli, F. Ferrari, A. Berardi, L. Mughetti

2018/9 — pag. 561-568

After the first trimester of pregnancy future parents are commonly asked if their child will be male or female. Such a question creates many expectations and implies the true determination of the baby's identity. Indeed, since the earliest stages of ...

RI Aggiornamento
Insufficienza surrenalica: rara ma non troppo

G. Patti, G. Tornese, M.C. Pellegrin, K. Vecchiato, E. Faleschini, A. Ventura

2016/1 — pag. 21-26

Adrenal insufficiency is a rare condition in childhood. Clinical characteristics of adrenal insufficiency in children may be non-specific. Therefore, the diagnosis may be suspected late. If unrecognized, adrenal insufficiency may present with life-...

RI Rubrica iconografica
Una tumefazione del clitoride

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

2014/2 — pag. 113-115

RI Percorsi clinici
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...

RI Pagine elettroniche
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...

EL Caso contributivo
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...

RI Percorsi clinici
Un lattante distrofico con alcalosi metabolica

L. Calligaris, G. Cont, D. Codrich, F. Zennaro, F. Marchetti

2006/2 — pag. 111-114

We describe a case of a 4 months-old girl who come to our attention because of an history of failure to thrive and recurrent vomiting started during the second month of life; only remarkable laboratory data were the presence of hyponatriemia and hypo...

EL Caso Clinico Interattivo
Accesso libero
Un lattante distrofico

L. Calligaris, G. Cont, D. Codrich, F. Zennaro, F. Marchetti

2005/9

EL Caso Clinico Interattivo
Accesso libero
Un lattante distrofico

L. Calligaris, G. Cont, D. Codrich, F. Zennaro, F. Marchetti

2005/9

RI Aggiornamento monografico
Sindrome adreno-genitale congenita da deficit di 21-idrossilasi

A. Balsamo, A. Cicognani

2005/5 — pag. 293-301

Congenital adrenal hyperplasia (CAH) refers to a group of inherited disorders of adrenal steroidogenesis. More than 90% of CAH is due to 21-hydroxylase deficiency (21-OH-D), found in 1:10.000 to 1:15.000 live births as classical form and detected i...

RI Linee guida
DOCUMENTO DI INDIRIZZO Le urgenze endocrinologiche

G. Tonini, et al.

2003/9 — pag. 590-595

Many endocrinological disease represent, in particular conditions, a real emergency. Thireotoxicosis in Graves disease, adrenal insufficiency secondary to acute adrenal dysfunction, surgical intervention or acute disease in a SAG affected patients,...