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USMLE Step 1 First Aid Rapid Review 2026 | Medical School Exam Prep | Verified Questions & Answers for Anatomy, Physiology & Pathology

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Prepare efficiently for USMLE Step 1 (2026) with this rapid review study guide based on the trusted First Aid for the USMLE Step 1. This resource provides high-yield summaries, key facts, and exam-focused concepts designed to help medical students maximize retention and improve performance on Step 1. The guide covers essential topics including anatomy, physiology, biochemistry, microbiology, pharmacology, pathology, and behavioral sciences, all presented in a concise format ideal for rapid revision. It is structured to help students focus on high-yield content frequently tested in the USMLE Step 1 exam. This resource is ideal for medical students preparing for Step 1, providing a reliable tool to reinforce knowledge, streamline review, and enhance exam readiness.

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USMLE Step 1 First Aid Rapid Review
2026 | Medical School Exam Prep |
Verified Questions & Answers for
Anatomy, Physiology & Pathology

Abdominal pain, ascites, hepatomegaly -- Verified--Solution----Budd-
Chiari Syndrome (post hepatic venous thrombosis). Associated with
Polycythemia vera.


Achilles tendon Xanthoma -- Verified--Solution----Familial
Hypercholesterolemia (absent/defective LDL receptors)
May have MI before age 20
Autosomal dominant


Adrenal hemorrhage, hypotension, DIC -- Verified--Solution----
Waterhouse-Friedrichsen syndrome (Neisseria meningitidis)


Anaphylaxis and/or angioedema following blood transfusion -- Verified-
-Solution----IgA deficiency; C1 inhibitor deficiency would only cause
angioedema, not anaphylaxis


Arachnodactyly (spider fingers), lens dislocation, aortic dissection or
aneurysm, hyperflexible joints, pectus excavatum -- Verified--Solution--
--Marfan Syndrome (FBN1 gene mutation

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chromosome 15 leads to defective fibrillin)
Autosomal Dominant


Athlete with polycythemia -- Verified--Solution----Secondary to EPO
injection


Back pain, fever, night sweats -- Verified--Solution----Pott disease
(vertebral TB)


Bilateral acoustic schwannomas -- Verified--Solution----
Neurofibromatosis type 2
S-100+, cerebellopontine angle


Bilateral hilar adenopathy, uveitis, high ACE, hypercalcemia (activated
macrophages for Vit D), interstitial fibrosis, erythema nodosum,
elevated CD4:CD8 ratio on lavage; asteroid bodies -- Verified--
Solution----Sarcoidosis (non-caseating granulomas)


Black eschar on face of patient with diabetic ketoacidosis -- Verified--
Solution----Mucor or Rhizopus fungal infection
Travels through cribiform plate vessels


Blue sclera -- Verified--Solution----Osteogenesis Imperfecta (Type I
collagen defect forming triple helix)
Blue due to exposure of choroidal veins

,3 | Page


Bluish line on gingiva and basophilic stippling -- Verified--Solution----
Burton line (lead poisoning)
Basophilic stippling (rRNA remnants)
Constipation, anemia, CNS impairment


Bone pain, bone enlargement (hat size or hearing loss), arthritis --
Verified--Solution----Paget disease of bone (Increased osteoclastic, then
osteoblastic activity)
Osteosarcoma or heart failure


Bounding pulses, wide pulse pressure, diastolic heart murmur, head
bobbing -- Verified--Solution----Aortic Regurgitation


"Butterfly" facial rash or discoid rash and Raynaud phenomenon in a
young female -- Verified--Solution----Systemic lupus erythematosus
Type III Hypersensitivity (antigen-antibody complexes deposit) with
glomerulonephritis
Type II hypersensitivity with autoimmune hemolysis


Carcinoma spread -- Verified--Solution----Lymphatics to lymph nodes
(except HCC, Renal cell, follicular thyroid and choriocarcinoma which
spread hematogenously)


Sarcoma spread -- Verified--Solution----Hematogenously

, 4 | Page


Cafe-au-lait spots, Lisch nodules (iris hemartoma), cutaneous
neurofibromas -- Verified--Solution----Neurofibromatosis Type I,
pheochromocytoma, optic gliomas


Cafe-au-lait spots (unilateral), polyostotic fibrous dysplasia, precocious
puberty, multiple endocrine abnormalities -- Verified--Solution----
McCune-Albright syndrome (mosaicism, G-protein signaling mutation)


Calf pseudohypertrophy -- Verified--Solution----Muscular dystrophy
(Duchenne, due to X-linked frameshift > truncated dystrophin)
Dilated cardiomyopathy
High CK


Cervical lymphadenopathy, desquamating rash on palms and soles,
coronary aneurysms, red conjuctivae, and strawberry tongue -- Verified-
-Solution----Kawasaki disease (treat with IVIG and aspirin which
inhibits TXA2)


"Cherry-red spots" on macula -- Verified--Solution----Tay-Sachs
(ganglioside accumulation - NO hepatosplenomegaly)
Niemann-Pick (sphingomyelin accumulation)
Central retinal artery occlusion


Chest pain on exertion -- Verified--Solution----Angina (stable: with
moderate exertion, *cellular swelling indicates reversibility*,

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