| 词条 | Haemochromatosis type 3 |
| 释义 |
| name = Haemochromatosis type 3 | synonyms = | image = | caption = | pronounce = | field = hematology | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }}Haemochromatosis type 3 is a type of Iron overload disorder associated with deficiencies in transferrin receptor 2. It exhibits an autosomal recessive inheritance pattern.[1][2][3] References1. ^{{cite journal |vauthors=Roetto A, Totaro A, Piperno A, etal |title=New mutations inactivating transferrin receptor 2 in hemochromatosis type 3 |journal=Blood |volume=97 |issue=9 |pages=2555–60 |date=May 2001 |pmid=11313241 |doi= 10.1182/blood.V97.9.2555}} 2. ^{{cite journal |vauthors=Roetto A, Daraio F, Alberti F, etal |title=Hemochromatosis due to mutations in transferrin receptor 2 |journal=Blood Cells Mol. Dis. |volume=29 |issue=3 |pages=465–70 |year=2002 |pmid=12547237 |doi= 10.1006/bcmd.2002.0585}} 3. ^{{cite journal |vauthors=Roetto A, Camaschella C |title=New insights into iron homeostasis through the study of non-HFE hereditary haemochromatosis |journal=Best Pract Res Clin Haematol |volume=18 |issue=2 |pages=235–50 |date=June 2005 |pmid=15737887 |doi=10.1016/j.beha.2004.09.004 |url=http://linkinghub.elsevier.com/retrieve/pii/S1521-6926(04)00096-9}} External links{{Medical resources| DiseasesDB = | ICD10 = E83.1 | ICD9 = | ICDO = | OMIM = 604250 | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = C537248 | Orphanet = 225123 }}{{Inborn errors of metal metabolism}}{{blood-disease-stub}}{{genetic-disorder-stub}} 2 : Iron metabolism|Red blood cell disorders |
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