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Rametta, Raffaela

About me

Name: Raffaela

Surname: Rametta

Academic title: dr.


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):

Molecular Diagnosis

Diseases:

Rare hereditary hemochromatosis HFE related hereditary hemochromatosis Symptomatic form of hemochromatosis type 1 (OMIM 235200) Hemochromatosis due to rare mutations in HFE (OMIM 235200) Non-HFE related hereditary hemochromatosis Hemochromatosis type 2(OMIM 602390, 613313) Hemochromatosis type 2A (OMIM 602390) Hemochromatosis type 2B (OMIM 613313) Hemochromatosis type 3 (OMIM 604250) Hemochromatosis type 5 (OMIM 615517) Hemochromatosis type 4B (OMIM 606069) Ferroportin Disease Hemochromatosis type 4A (OMIM 606069)

Which is your patient age coverage?

  • Adults


Subnetwork representative:

  • HH-Iron

Member Go to member

Name english: Foundation IRCCS Ca’Granda Ospedale Maggiore Policlinico, Milan

Name original: Fondazione IRCCS CA'Granda Ospedale Maggiore Policlinico , Milano


Healthcare provider Go to healthcare provider

Name english: Foundation IRCCS Ca’Granda Ospedale Maggiore Policlinico, Milan

Name original: Fondazione IRCCS CA'Granda Ospedale Maggiore Policlinico , Milano

Departments

English name Original name Subnetworks of expertise Healthcare provider