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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) HJV related hereditary hemochromatosis - OMIM 602390 (Hemochromatosis type 2A) HAMP related hereditary hemochromatosis - OMIM 613313 (Hemochromatosis type 2B) TFR2 related hereditary hemochromatosis OMIM 604250 (Hemochromatosis type 3) FTH related hereditary hemochromatosis - OMIM 615517 (Hemochromatosis type 5) Ferroportin Disease (Hemochromatosis type 4B)​ SLC40A1 related hereditary hemochromatosis - OMIM 606069 (Hemochromatosis type 4A)

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