ResoundingHealth
Search
  
Fanconi's Anemia


Is a Disease or Syndrome.

"Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650, August 20, 2004)"

Related Topics

The following genes (and their mutations) are connected to this condition:
FANCJBRIP1BACH1
FANCL
FANCM
FANCM
FANCN
FANCI
FANCE
FANCF
FANCG
FANCG
PALB2
FANCA
FANCB
FANCC
BRIP1
BRIP1
BRCA2
BRCA2
BRCA2
BRCA2
BRCA2
BRCA2
BRCA2
BRCA2
FANCD2
FANCD1

Related Medication
The following information has been extracted from US Food and Drug Administration databases. It shows drugs which may be used to treat this condition, and those drugs whose use may be dangerous with this condition. This is informational only. You must consult a physician for your particular case. You may click on a listed drug for further information.

The following medications may be hazardous when used with this condition

Vistide

This web-site is for informational purposes only and is not intended as a substitute for advice from your doctor. It should not to be used for self-diagnosis or treatment.