Hereditary Angioedema with Normal C1 Inhibitor

American Journal of Medicine

Volumn 121, Issue 11, 2008, Pages 949-951

  Patel, Nilesh N ^a   Patel, Devesh N ^b  

^a Citrus Valley Medical Center   (United States)

^b ROGER WILLIAMS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FERROUS FUMARATE; FERROUS GLUCONATE; FERROUS SULFATE; IRON;

ARTICLE; CONSTIPATION; DIARRHEA; DIET SUPPLEMENTATION; DRUG ABSORPTION; DRUG FORMULATION; DRUG TOLERABILITY; EPIGASTRIC DISCOMFORT; HUMAN; IRON DEFICIENCY ANEMIA; IRON THERAPY; MULTIPLE CYCLE TREATMENT; NAUSEA; PRIORITY JOURNAL; TREATMENT FAILURE;

EID: 54349093011     PISSN: 00029343     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.amjmed.2008.06.042     Document Type: Note

References (11)

1. Temino V.M., and Peebles R.S. The spectrum and treatment of angioedema. Am J Med 121 (2008) 282-286 4
2. Nzeako U., Frigas E., and Tremaine W.J. Hereditary angioedema: a broad review for clinicians. Arch Intern Med 161 (2001) 2417-2429 20
3. Bowen T., Cicardi M., Farkas H., et al. Canadian 2003 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema. J Allergy Clin Immunol 114 (2004) 629-637
4. Bork K., Barnstedt S.E., Koch P., and Traupe H. Hereditary angioedema with normal C1-inhibitor activity in women. The Lancet 56 (2000) 213-217
5. Binkley K.A., and Davis A. Clinical, biochemical, and genetic characterization of a novel estrogen dependent inherited for angioedema. J Allergy Clin Immunol 106 (2000) 546-550
6. Bork K., Gul D., Hardt J., and Dewald G. Hereditary angioedema with normal C1 inhibitor: clinical symptoms and course. Am J Med 120 (2007) 987-992 11
7. Dewald G., and Bork K. Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor. Biochem Biophys Res Commun 343 (2006) 1286-1289
8. Cichon S., Martin L., Hennies H.C., et al. Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III. Am J Hum Genet 79 (2006) 1098-1104
9. Bork K., Gul D., and Dewald G. Hereditary angio-oedema with normal C1 inhibitor in a family with affected women and men. Brit J Derm 154 (2006) 542-545 3
10. Martin L. Hereditary angioedema with normal C1 inhibitor gene in a family with affected women and men is associated with the p.Thr328Lys mutation on the F12 gene. J Allergy Clin Immunol 120 (2007) 975-977 4
11. Gupta S., Yu F., and Klaustermeyer W.B. New variant hereditary angioedema in three brothers with normal C1 esterase inhibitor level and function. Allergy 59 (2004) 557-558