hereditary spherocytosis

Le colelitiasi a origine ematologica

Fantasia M, Faraguna MC, Ferrari GM, Corti P.

2024/3 — pag. 187 — DOI

A 7-year-old girl presenting with acute abdominal pain due to gallstones was eventually diagnosed with spherocytosis....

Sferocitosi: una famiglia... tre malattie!

Ferrara D, Giordano C, Borsellino Z, Cuccia L, Ruffo GB, Corsello G.

2024/1 — pag. 54-57 — DOI

The paper describes the cases of three siblings affected by Hereditary Spherocytosis (HS). The different clinical presentations in the same family are examples of the heterogeneity of this pathology. HS is a common inherited type of haemolytic anaemi...

Sferocitosi: una famiglia... tre malattie!

Ferrara D, Giordano C, Borsellino Z, Cuccia L, Ruffo GB, Corsello G

2024/1 — pag. 5-8 — DOI

The paper describes the cases of three siblings affected by Hereditary Spherocytosis (HS). The different clinical presentations in the same family are examples of the heterogeneity of this pathology. HS is a common inherited type of haemolytic anaemi...

Secondo i miei “calcoli”... non è una gastrite

Arnaboldi S, Quattrocchi G, Ferrari GM, Corti P

2022/6 — pag. 129-130 — DOI

The case of an 11-year-old girl affected by hereditary spherocytosis admitted to hospital for abdominal pain is described. The diagnosis of cholelithiasis was eventually made....

Un’anemia emolitica da sferocitosi ereditaria

Ursi D, Valentino MS

2021/3 — pag. 193-195 — DOI

A case of haemolytic anaemia due to spherocytosis in a 3-month-old infant is reported. It is important to remember that post-transfusion blood tests are not reliable and must be repeated 3 months after the transfusion. The erythrocyte osmotic resista...

Sindrome di Morquio e sferocitosi ereditaria

S.M.C. Gramaglia, M. Lo Presti, C. Casà, G. Gramaglia

2020/10 — pag. 248-251 — DOI

Metabolic diseases are rare genetic conditions in the paediatric age. The diagnostic process is often complex and the diagnosis comes even years after the onset of symptoms. The article presents the only documented case of Morquio syndrome and heredi...

Quando la sferocitosi incontra il chirurgo

C. Bibalo

2015/6 — pag. 391-392

Summary Hereditary spherocytosis is a common inherited disorder that is characterized by anaemia, jaundice and splenomegaly. It is reported worldwide and is the most common inherited anaemia in individuals of northern European ancestry. Clinical ...

Quando la sferocitosi incontra il chirurgo

C. Bibalo

2015/6

Summary Hereditary spherocytosis is a common inherited disorder that is characterized by anaemia, jaundice and splenomegaly. It is reported worldwide and is the most common inherited anaemia in individuals of northern European ancestry. Clinical ...

Precisazioni sull’emocromoFluoroprofilassiAncora sul costo dei latti!

2004/7 — pag. 423

Una caso di mielodisplasia... da parvovirus!

E. Barth, G.A. Zanazzo, M. Rabusin, P. Tamaro

2002/1