Definitions & Key takeaways
Bloom syndrome is a rare autosomal recessive genetic disorder caused by a mutation in the BLM gene. It is characterized by small stature, a distinctive facial appearance, immunodeficiency, and increased susceptibility to cancer. Most people with Bloom syndrome die in their early twenties, usually from cancer or respiratory problems.
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Lysosomal storage disorders: Pathology review
Osteogenesis imperfecta
Familial hypercholesterolemia
Gene regulation
Epigenetics
Cell cycle
DNA damage and repair
Mitosis and meiosis
DNA mutations
Karyotyping
Mendelian genetics and punnett squares
Inheritance patterns
Independent assortment of genes and linkage
Huntington disease
Sickle cell disease (NORD)
Beta-thalassemia
Ehlers-Danlos syndrome
Extracellular matrix
Vitamin C deficiency
Myasthenia gravis
Cholinomimetics: Indirect agonists (anticholinesterases)
Neuromuscular junction disorders: Pathology review
Muscular dystrophy
Adrenergic receptors
Adrenergic antagonists: Alpha blockers
Adrenergic antagonists: Beta blockers
Adrenergic antagonists: Presynaptic
Sympathomimetics: Direct agonists
Muscarinic antagonists
Cholinergic receptors
Rett syndrome
Prader-Willi syndrome
Angelman syndrome
Cholinomimetics: Direct agonists
Purine and pyrimidine synthesis and metabolism disorders: Pathology review
Nucleotide metabolism
Gout and pseudogout: Pathology review
Gout
Adenosine deaminase deficiency
Hypokinetic movement disorders: Clinical
Multiple sclerosis
Demyelinating disorders: Pathology review
Muscle contraction
Skeletal muscle histology
Cardiac muscle histology
Sliding filament model of muscle contraction
Introduction to pharmacology
Pharmacodynamics: Drug-receptor interactions
Pharmacodynamics: Desensitization and tolerance
Pharmacodynamics: Agonist, partial agonist and antagonist
Pharmacokinetics: Drug absorption and distribution
Pharmacokinetics: Drug metabolism
Pharmacokinetics: Drug elimination and clearance
Oncogenes and tumor suppressor genes
DNA cloning
DNA synthesis inhibitors: Fluoroquinolones
Macrocytic anemia: Pathology review
Ataxia-telangiectasia
Colorectal polyps
Breast cancer: Pathology review
Necrosis and apoptosis
Atrophy, aplasia, and hypoplasia
Non-Hodgkin lymphoma
Fluorescence in situ hybridization
Parasympathetic nervous system
Sympathetic nervous system
Nervous system anatomy and physiology
Introduction to the somatic and autonomic nervous systems
Central nervous system histology
Peripheral nervous system histology
Muscular system anatomy and physiology
Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD)
Marfan syndrome
Bloom syndrome
Fragile X syndrome
Williams syndrome
Phenylketonuria (NORD)
Pheochromocytoma
Hardy-Weinberg equilibrium
Lac operon
Myotonic dystrophy
Cri du chat syndrome
Xeroderma pigmentosum
Beckwith-Wiedemann syndrome
Extracellular matrix
Kwashiorkor
Marasmus
Horner syndrome