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Nondisjunction
Error in cell division where homologous chromosomes or sister chromatids fail to separate properly, leading to aneuploidy.
Polyploidy
Presence of more than two complete sets of chromosomes in a cell, often seen in plants and associated with developmental disorders in humans.
Inflammation
Body's response to injury or infection, characterized by acute and chronic phases involving different immune cells and mediators.
Cell Adaptation
Cellular responses to stress or changes, including atrophy, hypertrophy, hyperplasia, metaplasia, and dysplasia.
Meiosis
Specialized cell division process producing haploid gametes with genetic diversity through crossing over and independent assortment.
Neural Stem Cells
Multipotent cells in the nervous system capable of differentiating into neurons, astrocytes, and oligodendrocytes, crucial for neurodevelopment and repair.
Active Transport
Movement of molecules against their concentration gradient requiring energy, exemplified by processes like the sodium-potassium pump.
Diffusion
Passive movement of molecules from high to low concentration, essential for processes like gas exchange and nutrient uptake.
Osmosis
Diffusion of water through a selectively permeable membrane from low to high solute concentration, crucial for fluid balance.
Turner's Syndrome
Genetic disorder in females characterized by monosomy X, leading to various physical and reproductive abnormalities.
Fragile X Syndrome
Genetic disorder caused by CGG triplet repeat expansion on the X chromosome, resulting in intellectual disability and physical features.
Cystic Fibrosis
Autosomal recessive disorder affecting chloride channels, leading to mucus accumulation and impacting respiratory and digestive systems.
Huntington's Disease
Autosomal dominant neurodegenerative disorder caused by CAG repeat expansion in the HTT gene, leading to motor and cognitive symptoms.
Homologous Chromosomes
Chromosome pairs with the same genes, one from each parent, important for genetic diversity through recombination during meiosis.
Autosomal Recessive Disorders
Disorders requiring mutations in both alleles of a gene for manifestation, exemplified by conditions like cystic fibrosis.
Autosomal Dominant Disorders
Disorders manifesting with a mutation in one allele of a gene, such as Huntington's disease, with a 50% chance of inheritance.
X-linked Disorders
Disorders caused by mutations in genes on the X chromosome, including conditions like hemophilia A and Duchenne muscular dystrophy.
Epigenetic Effects
Heritable changes in gene expression that do not involve changes to the DNA sequence.
DNA Methylation
Addition of methyl groups to cytosine residues, often silencing gene expression.
Histone Modification
Post-translational modifications of histone proteins affecting chromatin structure and gene expression.
Immunopathology/Infection
The study of diseases related to the immune system and the effects of infections on the body.
Innate Immunity
Non-specific first line of defense including physical barriers, phagocytes, and innate immune proteins.
Active Immunity
Immunity acquired through exposure to antigens, leading to memory cell formation and long-lasting protection.
Passive Immunity
Transfer of antibodies from another individual providing temporary protection.
IgG
Most abundant antibody in circulation, conferring long-term protection and crossing the placenta.
IgM
First antibody produced during an immune response, effective at forming antigen-antibody complexes.
IgE
Antibody involved in allergic reactions and defense against parasitic infections.
Mast Cells
Cells that release histamine and other mediators contributing to inflammation and allergic responses.
Indirect Transmission
Transmission of infectious agents through an intermediary like a vector or fomite.
T Lymphocytes
Key players in cell-mediated immunity, including helper T cells and cytotoxic T cells.
B Lymphocytes
Responsible for humoral immunity, producing antibodies and memory B cells.
Urticaria
Also known as hives, characterized by red, itchy welts on the skin due to allergic reactions.
Eosinophils
Granulocytes combating parasitic infections and allergic reactions by releasing toxic proteins.
Neutrophils
Most abundant white blood cells, first responders to infection performing phagocytosis.
Monocytes
Blood cells that become macrophages and dendritic cells, key in phagocytosis and antigen presentation.
Leukotrienes
Lipid mediators produced by leukocytes, promoting inflammation and chemotaxis.
Natural Killer (NK) Cells
Lymphocytes that recognize and kill virus-infected cells and tumors without prior sensitization.
Basophils
Granulocytes involved in allergic reactions, releasing histamine and other mediators.
Acid-base Balance
Maintenance of the equilibrium between acid and base concentrations in the body.
Metabolic Acidosis
Acidosis caused by excess hydrogen ions or loss of bicarbonate, leading to decreased pH.
Metabolic Alkalosis
Alkalosis caused by loss of hydrogen ions or gain of bicarbonate, leading to increased pH.
Respiratory Acidosis
Acidosis due to decreased alveolar ventilation leading to CO2 retention.
Respiratory Alkalosis
Alkalosis due to increased alveolar ventilation leading to CO2 loss.
CO Poisoning
Poisoning caused by carbon monoxide binding to hemoglobin, impairing oxygen delivery.
Strangulation
Obstruction of air or blood flow in the neck leading to hypoxia.
Asphyxiation
Insufficient oxygen intake causing hypoxia, with symptoms like cyanosis and confusion.
Dehydration
Excessive loss of body water leading to symptoms like thirst and decreased urine output.
Tetanus Toxoids
Vaccines containing inactivated tetanus toxin to provide immunity against tetanus.