Skip to the video

Fanconi anemia

Foundational SciencesCellular and molecular biologyMolecular biologyDisorders of molecular biologyDNA replication and repair disorders
Foundational SciencesGeneticsMolecular biologyDisorders of molecular biologyDNA replication and repair disorders
Foundational SciencesPathologyBlood and lymphoreticular systemAnemia, cytopenias, and polycythemia anemiasMegaloblastic macrocytic anemia
Foundational SciencesPathologyBlood and lymphoreticular systemAnemia, cytopenias, and polycythemia anemiasNon-megaloblastic macrocytic anemia
Organ SystemsBlood and lymphoreticular systemPathologyAnemia, cytopenias, and polycythemia anemiasMegaloblastic macrocytic anemia
Organ SystemsBlood and lymphoreticular systemPathologyAnemia, cytopenias, and polycythemia anemiasNon-megaloblastic macrocytic anemia

Definitions & Key takeaways

Fanconi anemia (FA) is an autosomal recessive disorder in which there is decreased production of red blood cells (anemia), white blood cells, and platelets due to bone marrow failure. This can cause problems with the immune system, increase the risk of infection, and can lead to bleeding problems. People with FA may also have stature, upper limb malformations, and an increased incidence of acute myeloid leukemia.

High Yield NotesAssessmentsMy Notes

No notes for this video yet

Try adding a note below

Ask Osmosis AI

Grounded in trusted Elsevier sources-- not the open web

Tutor me on this

Build clinical reasoning, Socratic-style.

Trial

Explain this simply

Get clearer explanations of difficult concepts.

Trial

Summarize high-yield points

Review what matters most for exams.

Trial

Quiz me with 3 questions

Practice active recall for exam prep after watching.

Trial

Try the full Osmosis experience

Watch the full video

Ask Osmosis AI questions

Generate practice questions

Get 1-on-1 AI tutoring

Create a personalized study schedule

See plans

Related

Up next

Acute radiation syndrome

Acute radiation syndrome

Anemias

Diamond-Blackfan anemia
Fanconi anemia
Autoimmune hemolytic anemia
Extrinsic hemolytic normocytic anemia: Pathology review
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Hemolytic disease of the newborn
Hereditary spherocytosis
Intrinsic hemolytic normocytic anemia: Pathology review
Paroxysmal nocturnal hemoglobinuria
Pyruvate kinase deficiency
Sickle cell disease (NORD)
Fanconi anemia
Folate (Vitamin B9) deficiency
Megaloblastic anemia
Vitamin B12 deficiency
Alpha-thalassemia
Anemia of chronic disease
Beta-thalassemia
Iron deficiency anemia
Lead poisoning
Sideroblastic anemia
Microcytic anemia: Pathology review
Anemia of chronic disease
Aplastic anemia
Non-hemolytic normocytic anemia: Pathology review
Macrocytic anemia: Pathology review

Coagulation disorders

Hemophilia
Vitamin K deficiency

Dysplastic and proliferative disorders

Langerhans cell histiocytosis
Mastocytosis (NORD)
Essential thrombocythemia (NORD)
Myelodysplastic syndromes
Myelofibrosis (NORD)
Myeloproliferative disorders: Pathology review
Polycythemia vera (NORD)

Heme synthesis disorders

Acute intermittent porphyria
Heme synthesis disorders: Pathology review
Lead poisoning
Porphyria cutanea tarda

Leukemias

Acute leukemia
Chronic leukemia
Leukemias: Pathology review

Leukemoid reaction

Leukemoid reaction

Lymphomas

Hodgkin lymphoma
Lymphomas: Pathology review
Non-Hodgkin lymphoma

Mixed platelet and coagulation disorders

Coagulation disorders: Pathology review
Disseminated intravascular coagulation
Heparin-induced thrombocytopenia
Mixed platelet and coagulation disorders: Pathology review
Von Willebrand disease

Plasma cell dyscrasias

Monoclonal gammopathy of undetermined significance
Multiple myeloma
Plasma cell disorders: Pathology review
Waldenstrom macroglobulinemia

Platelet disorders

Bernard-Soulier syndrome
Glanzmann's thrombasthenia
Hemolytic-uremic syndrome
Immune thrombocytopenia
Platelet disorders: Pathology review
Thrombotic thrombocytopenic purpura

Thrombosis syndromes

Antiphospholipid syndrome
Antithrombin III deficiency
Factor V Leiden
Protein C deficiency
Protein S deficiency
Thrombosis syndromes (hypercoagulability): Pathology review
Osmosis from Elsevier logo

Exams

  • USMLE 1+2
  • COMLEX 1+2
  • PANCE
  • NCLEX
  • UKMLA
  • ABFM/ABIM

Pricing

  • Medicine (MD)
  • Medicine (DO)
  • Nurse Practitioner
  • Physician Assistant
  • Registered Nurse
  • Licensed Practical Nursing
  • Dentistry
  • Pharmacy
  • Health Professional

Follow us

  • YouTube
  • LinkedIn
  • Facebook
  • Instagram (Medical)
  • Instagram (Nursing)
  • Bluesky
  • Twitter
  • TikTok

Company

  • About Us
  • Careers
  • Press
  • Contact us

Resources

  • Library
  • Blog
  • Events
  • Podcast
  • Help Center

For institutions

  • Institutions
Elsevier

Copyright © 2026 Elsevier, its licensors, and contributors. All rights are reserved, including those for text and data mining, AI training, and similar technologies.

Cookies are used by this site.

Terms and Conditions

|

Privacy Policy

|

Cookie Notice

|

Sitemap

USMLE® is a joint program of the Federation of State Medical Boards (FSMB) and the National Board of Medical Examiners (NBME). COMLEX-USA® is a registered trademark of The National Board of Osteopathic Medical Examiners, Inc. NCLEX-RN® is a registered trademark of the National Council of State Boards of Nursing, Inc. Test names and other trademarks are the property of the respective trademark holders. None of the trademark holders are endorsed by nor affiliated with Osmosis or this website.