Family History

Pigmenti fuori posto: indizi per una diagnosi rara

Sarno E, Cecconi I

2026/5 — pag. 131-132 — DOI

The paper presents the clinical case of a young girl initially diagnosed with cutaneous mastocytosis based on early skin lesions. However, the persistence of hyperpigmented macules over three years, the development of scarring alopecia, dental agenes...

L’autolesionismo non suicidario

Ronconi M

2026/1 — pag. 17-19 — DOI

This case study focuses on a 14-year-old girl presenting with self-harming behaviours, reported as a means to cope with deep emotional emptiness. Despite high academic achievement and advanced language skills, her clinical history reveals long-standi...

Emergenze neurologiche: caccia all'imitatrice

Corona L, Mazza S, Cualbu A

2024/3 — pag. 189-192 — DOI

The case of a 13-year-old girl presenting with a panic attack following a sudden onset of headache and weakness in the lower right limb is described. Hemiplegic migraine was eventually diagnosed....

Chi va con lo zoppo...

Venditto L, Ciarletta R, La Fauci G.

2022/3 — pag. 189-192 — DOI

A familial case of Perthes disease is described. The clinical presentation and the diagnostic approach to this disease are discussed....

Modi diversi di sviluppare un diabete

M. Pavan, A. Lora, G. Gortani, E. Faleschini

2017/6 — pag. 395-396

Una sera come tutte le altre!

A. Marzano

2010/4

Storia di una famiglia con sindrome di Peutz-Jeghers: importanza dello screening strumentale anche nei soggetti asintomatici

2003/9 — pag. 606

Report on two brothers with PJS and a positive family history. The first one symptomatic from when was 16 months; the second one asymtomatic underwent to EGDS when fifteen and after endoscopic removal of 6 polyps (the biggest >3 cm) develop emorra...