Sensorineural hearing loss

Ematuria e non solo... a volte è questione di famiglia: la sindrome di Alport

Sarno E, Alberici I, La Scola C, Pillon R, Pasini A

2025/3 — pag. 72-72 — DOI

The paper reports the case of a 4-year-old girl with recurrent episodes of macrohematuria. Her family history revealed renal and ocular anomalies. Clinical and genetic analyses confirmed X-linked compound heterozygosity for Alport syndrome, with two ...

La sindrome di Stickler

Cazzaniga L, Abramo M, Selicorni A.

2024/4 — pag. 251-253 — DOI

Infezione congenita da citomegalovirus e ipoacusia

Gambacorta V, Orzan E, Lapenna R, Ricci G

2022/10 — pag. 195-199 — DOI

Background - Cytomegalovirus (CMV) infection is the most common of congenital infections, with a prevalence of 0.3-1.2% in industrialized countries and is the most frequent non-genetic cause of permanent hearing loss in children, with an incidence ra...

Ogni età ha la sua macroematuria

Delcaro G, Pennesi M.

2022/9 — pag. 598-600 — DOI

A girl with gross haematuria was finally diagnosed with X-linked Alport syndrome that was initially diagnosed as Berger syndrome. The clinical implication of X-linked Alport syndrome is discussed....

L’inquadramento delle ipoacusie in epoca neonatale e pediatrica

A. Feresin, M. Bevacqua, G. Del Piero, P. Staffa, E. Barbi, E. Orzan

2020/8 — pag. 505-511 — DOI

Conductive, mild-moderate hearing impairment in children is a very frequent condition after newborn hearing screening that easily leads to misdiagnosis. Conductive hearing impairment needs an accurate differential diagnosis to avoid inadequate treatm...

Sindrome di Waardenburg

S. Tajè, M.C. Provero, P. Cianci, A. Selicorni

2019/3 — pag. 185-187

La sindrome CHARGE

S. Tajè, P. Cianci, A. Selicorni

2017/9 — pag. 585-586

Sindrome di Waardenburg: descrizione di un caso clinico

V. Carrato, A. Spinelli, I. Bruno

2017/5 — pag. 323-324

Waardenburg syndrome - type 1 (WS1) is an autosomal dominant disease clinically and genetically heterogeneous. It is characterized by non-progressive sensorineural hearing loss of variable degree and anomalous pigmentation of the eyes and the skin ca...

Sindrome di Waardenburg - Descrizione di un caso clinico

V. Carrato, A. Spinelli, I. Bruno

2017/5

Waardenburg syndrome - type 1 (WS1) is an autosomal dominant disease clinically and genetically heterogeneous. It is characterized by non-progressive sensorineural hearing loss of variable degree and anomalous pigmentation of the eyes and the skin ca...

Screening e sorveglianza dell’ipoacusia in Friuli Venezia Giulia

M. Gregori

2016/6

L’impianto cocleare in età pediatrica: attuali indicazioni

F. Di Lella, A. Bacciu, E. Pasanisi, M. Guida, F. Canzano, V. Vincenti

2015/10

Cochlear implant is a partially implantable electronic device designed to provide profoundly deafened patients with hearing sensitivity within the speech range. Over the years patient candidacy has been expanded and the criteria for implantation cont...

La sindrome di Cornelia de Lange

2012/1 — pag. 58-59

Impianto cocleare per i bambini con gravi perdite dell'udito

G. Bartolozzi

2008/2

Giornata nazionale dell'infanzia e dell'adolescenzaGiornata infanzia, Napolitano: «Anche i rom vanno integrati»Mamme lavoratrici più felici di quelle a casaECM: quali novità all'orizzonte?Guerra agli sciroppi per la tosseObesità infantile: una maledizione di generazione in generazioneImpianti cocleari in bambini con sordità da grave a profonda

a cura Irene Bruno

2007/10

Lo screening neonatale per la sordità infantileMammismoLe scuole FAES e l’Opus Dei: tre lettere

1998/10 — pag. 649-651

L’ipoacusia neurosensoriale

D. Baronciani, A. Del Prete

1998/5 — pag. 327-329