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1,591 Possible Causes for Fanconi Anemia

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  • Endocrine Dysfunction

    Final short stature, found in five of the 35 patients who attained final height, was associated with the underlying disease (specifically, Fanconi anemia) (P 0.0013), previous[ncbi.nlm.nih.gov]

  • Sunburn

    Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia.[ncbi.nlm.nih.gov] Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia.[ncbi.nlm.nih.gov]

  • Myelodysplasia

    Fanconi anemia Familial MDS/AML ( GATA2 , DDX41 ) Thrombocytopenia 2 ( ANKRD26 ) Thrombocytopenia 5 ( ETV6 ) Familial aplastic anemia ( SRP72 ) Shwachman-Diamond syndrome[cancer.net] Hematologic abnormalities in Fanconi anemia: an International Fanconi Anemia Registry study. Blood . 1994 Sep 1. 84(5):1650-5. [Medline] .[emedicine.medscape.com] MDS occurs in 10-25% of individuals with this syndrome. [9] Fanconi anemia (4-7%) increases the risk of MDS and AML [10] ; 48% of patients with Fanconi anemia develop leukemia[emedicine.medscape.com]

  • Thrombocytopenia

    anemia May-Hegglin anomaly Acquired formation disorders Panmyelopathy Bone marrow diseases (e.g. leukemias ) Bone marrow damage Damage by medicines Toxic damage (e.g. lead[flexikon.doccheck.com] […] failure Sepsis, systemic viral or bacterial infection Leptospirosis Hereditary syndromes Congenital amegakaryocytic thrombocytopenia Thrombocytopenia absent radius syndrome Fanconi[en.wikipedia.org] Congenital causes of thrombocytopenia Von-Willibrand disease type 2B Wiskot-Aldrich syndrome Alport syndrome Fanconi’s anemia Bernard-Soulier syndrome Thrombocytopenia with[antimicrobe.org]

  • Developmental Disabilities

    People who have intellectual and developmental disabilities (IDD) often rely on caregivers to assist in the medication management process. The aim of this study was to learn from caregivers, who are either family or support staff, what major issues arise throughout the process of managing medication and how these[…][ncbi.nlm.nih.gov]

  • Obesity

    Sedentary lifestyles and increased pollution brought about by industrialization pose major challenges to the prevention of both obesity and chronic respiratory diseases such as chronic obstructive pulmonary disease (COPD), asthma, obstructive sleep apnea and obesity hypoventilation syndrome. Obesity has emerged[…][ncbi.nlm.nih.gov]

  • Fanconi Anemia

    Diagnosis of Fanconi anemia in patients without congenital malformations: an International Fanconi Anemia Registry study. Am J Med Genet 1996; 68: 58–61.[doi.org] A 3-year-old patient with Fanconi anemia.[emedicine.com] Phenotypic consequences of mutations in the Fanconi anemia FAC gene: an International Fanconi Anemia Registry study. Blood 1997; 90: 105–10. PubMed Google Scholar 19.[doi.org]

  • Congenital Aplastic Anemia

    Abstract Fanconi's anemia (FA) is an autosomal recessive disease manifested by pancytopenia resulting from bone marrow failure, variable physical anomalies and cancer susceptibility[ncbi.nlm.nih.gov] Comparison of several hematological and clinical parameters in Fanconi anemia (FA) (DEB ) and non-Fanconi anemia (non-FA)(DEB ) patients disclosed no statistically significant[ncbi.nlm.nih.gov] Fanconi anemia may be due to sequence anomalies affecting distinct genes involved in DNA repair. Fanconi anemia is the prime example for CAA.[symptoma.com]

  • Idiopathic Aplastic Anemia

    Abstract We have analyzed chromosome breaks in 8 patients with Fanconi anemia (FA), 42 with "idiopathic" aplastic anema (AA), 15 first-degree relatives of FA patients, and[ncbi.nlm.nih.gov] Abstract A cytogenetic test was developed to enable the diagnostic differentiation between Fanconi anemia and the group of disorders classified as "idiopathic" aplastic anemia[ncbi.nlm.nih.gov] […] accurate and timely diagnosis of Fanconi anemia to implement appropriate therapy.[ncbi.nlm.nih.gov]

  • Congenital Hypoplastic Anemia

    Associated genes include TERC, TERT, IFNG, NBS1, PRF1, and SBDS. [1] Examples include: Fanconi anemia Diamond-Blackfan anemia References [ edit ] Online Mendelian Inheritance[en.wikipedia.org] Abstract The authors identified persistent Th activation in five of seven children (71.4%) diagnosed as having Fanconi's anemia or Diamond-Blackfan syndrome.[ncbi.nlm.nih.gov] […] of Fanconi Anemia Patients Subtype A Recruiting NCT03157804 Phase 1, Phase 2 Plerixafor 39 Mobilization and Collection of Peripheral Blood Stem Cells in Patients With Fanconi[malacards.org]

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