Variants
Sign InSign Up

Fanconi anemia complementation group G

Your Results

Sign In

Description

Fanconi anemia (FA) is characterized by physical abnormalities, bone marrow failure, and increased risk for malignancy. Physical abnormalities, present in approximately 75% of affected individuals, include one or more of the following: short stature, abnormal skin pigmentation, skeletal malformations of the upper and/or lower limbs, microcephaly, and ophthalmic and genitourinary tract anomalies. Progressive bone marrow failure with pancytopenia typically presents in the first decade, often initially with thrombocytopenia or leukopenia. The incidence of acute myeloid leukemia is 13% by age 50 years. Solid tumors – particularly of the head and neck, skin, and genitourinary tract – are more common in individuals with FA.

GeneReviews

  • Mode of Inheritance

    VARIANTS

    142

    SEE THE VARIANTS →

    Genes

    External Links

    • OMIM

      614082

    • Orphanet
    • HPO
    • Medgen

      C3469527

    © 2024 Biocodify. All rights reserved.

    TwitterTwitter

    Product

    HomePricingDashboard

    Stay up to date

    The latest news and updates from Biocodify, sent to your inbox.