Members

Name: Roberta

Surname: Russo

Academic title: Researcher

Link to personal website:

https://www.docenti.unina.it/roberta.russo

Which is your area of expertise for the "Disease/group of diseases"?

• Diagnostics

Specify your expertise for the "Disease/group of diseases" (eg SCT, Molecular diagnosis):

Rare hereditary anemias/Congenital Dyserythropoietic Anemias, Molecular diagnosis, new causative genes discovery, research on pathogenetic mechanism of rare hereditary anemias

Diseases:

Thrombocytopenia with congenital dyserythropoietic anemia X-linked dyserythropoetic anemia with abnormal platelets and neutropenia Rare anemia Rare hemolytic anemia Rare constitutional hemolytic anemia Rare constitutional hemolytic anemia due to a red cell membrane anomaly Hereditary spherocytosis Hereditary elliptocytosis Distal renal tubular acidosis with anemia Hereditary stomatocytosis Overhydrated hereditary stomatocytosis Dehydrated hereditary stomatocytosis Rh deficiency syndrome Familial pseudohyperkalemia Southeast Asian ovalocytosis Hereditary cryohydrocytosis with reduced stomatin Hereditary cryohydrocytosis with normal stomatin Constitutional hemolytic anemia due to acanthocytosis Abetalipoproteinemia McLeod neuroacanthocytosis syndrome Primary CD59 deficiency Constitutional dyserythropoietic anemia Congenital dyserythropoietic anemia Congenital dyserythropoietic anemia type I Congenital dyserythropoietic anemia type III Congenital dyserythropoietic anemia type II Congenital dyserythropoietic anemia type IV

Which is your patient age coverage?

• Pediatrics
• Adults