Iris Diseases

Sindrome di Waardenburg

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

2019/3 — pag. 185-187

Un occhio più piccolo e uno più grande

P. Paganin

2018/4

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...

Quando il bambino non fissa lo sguardo

E. Rubinato, F. Parentin, G. Gortani, M. Spaccini

2010/6 — pag. 397-398

We report the case of a 2-month-old baby who was brought to our attention because his mother noted that he “doesn’t gaze” as his sister did. The child presented with absence of gazing movement and nistagmus. An ophtalmological evaluation revealed...

Sindrome di Waardenburg e sindrome del primo arco. Uno studio genealogico

1999/4