Hemochromatose et diabete.

Asthenia/etiology; Biopsy; Blood Glucose/analysis; Diabetic Diet; Diagnosis, Differential; Ferritins/blood; Glucose Tolerance Test; Hemochromatosis/diagnosis/genetics/metabolism/therapy; Humans; Hypoglycemic Agents/therapeutic use; Magnetic Resonance Imaging; Mass Screening/methods; Mutation/genetics; Phenotype; Phlebotomy; Time Factors; Transferrin/metabolism

Abstract :

[en] Nowadays, haemochromatosis is often diagnosed when the patient is monosymptomatic. Diabetes is frequently the first expression of the disease. So, it is important to know the clinical and biologic characteristics to evoke diagnosis as early as possible. Uncommon presentations request systematic screening.

Disciplines :

Endocrinology, metabolism & nutrition

Author, co-author :

Thielen, Vinciane ; Centre Hospitalier Universitaire de Liège - CHU > Diabétologie,nutrition, maladies métaboliques

Paquot, Nicolas ; Centre Hospitalier Universitaire de Liège - CHU > Diabétologie,nutrition, maladies métaboliques

Scheen, André ; Université de Liège - ULiège > Département des sciences cliniques > Diabétologie, nutrition et maladie métaboliques - Médecine interne générale

Language :

French

Title :

Hemochromatose et diabete.

Alternative titles :

[en] Hematochromatosis and diabetes

Publication date :

2004

Journal title :

Revue Médicale de Liège

ISSN :

0370-629X

eISSN :

2566-1566

Publisher :

Université de Liège. Revue Médicale de Liège, Liège, Belgium

Volume :

Issue :

Pages :

29-31

Peer reviewed :

Peer reviewed

Additional URL :

http://www.rmlg.ulg.ac.be

Available on ORBi :

since 08 May 2009

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Bibliography

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Kowdley KV, Tait JF, Bennett RL, et al.- Hereditary Hemochromatosis. Geneclinics, 2000, 151, 67-75.
Hanson EH, Imperatore G, Burke W.- HFE gene and hereditary hemochromatosis: review article. Am J Epidemiol, 2001, 154, 193-206.
Paris I, Hermans M, Buysschaert M.- Les complications endocriniennes de l'hémochromatose génétique. Acta Clin Belgica, 1999, 54, 334-345.
Barton JC, Sawada-Hirai R, Rothenberg BE, et al.- Two novel missense mutations of the HFE gene and identification of the S65C mutation in Alabama hemochromatosis probands. Blood Cells Mol Dis, 1999, 25, 147-155.
Buysschaert M, Paris I, Selvais PH.- Clinical aspects of diabetes secondary to idiopathic haemochromatosis in French-speaking Belgium. Diabetes Metab, 1997, 23, 308-331.
Yhouanq JM.- Diabetes and haemochromatosis: current concepts, management and prevention. Diabetes Metab, 1995, 21, 319-329.