Albinism

Last updated: November 01, 2022

Albinism

Term 1

Term 1

Glycolysis
Electron transport chain and oxidative phosphorylation
Glycogen metabolism
Citric acid cycle
Gluconeogenesis
Pentose phosphate pathway
Fatty acid oxidation
Fatty acid synthesis
Cholesterol metabolism
Ketone body metabolism
Amino acids and protein folding
Enzyme function
Amino acid metabolism
Nitrogen and urea cycle
Protein structure and synthesis
Cellular structure and function
Cell membrane
Selective permeability of the cell membrane
Extracellular matrix
Cell-cell junctions
Endocytosis and exocytosis
Osmosis
Resting membrane potential
Cell signaling pathways
Nuclear structure
Cytoskeleton and intracellular motility
Inflammation
Ischemia
Free radicals and cellular injury
Atrophy, aplasia, and hypoplasia
Metaplasia and dysplasia
Hyperplasia and hypertrophy
Oncogenes and tumor suppressor genes
DNA structure
Transcription of DNA
Translation of mRNA
DNA replication
DNA damage and repair
Cell cycle
Mitosis and meiosis
DNA mutations
Mendelian genetics and punnett squares
Inheritance patterns
Gene regulation
Epigenetics
Independent assortment of genes and linkage
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
Gel electrophoresis and genetic testing
DNA cloning
Galactosemia
Homocystinuria
Phenylketonuria (NORD)
Tay-Sachs disease (NORD)
Pyruvate dehydrogenase deficiency
Kwashiorkor
Marasmus
Folate (Vitamin B9) deficiency
Vitamin B12 deficiency
Down syndrome (Trisomy 21)
Patau syndrome (Trisomy 13)
Edwards syndrome (Trisomy 18)
Turner syndrome
Klinefelter syndrome
Ehlers-Danlos syndrome
Marfan syndrome
Myocardial infarction
Iron deficiency anemia
Alpha-thalassemia
Beta-thalassemia
Sickle cell disease (NORD)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Autoimmune hemolytic anemia
Introduction to pharmacology
Pharmacokinetics: Drug metabolism
Cystic fibrosis
Osteomalacia and rickets
Septic arthritis
Rheumatoid arthritis
Juvenile idiopathic arthritis
Gout
Osteoarthritis
Osteoporosis
Diabetes mellitus
Gestational diabetes
Lower urinary tract infection
Insomnia
Major depressive disorder
Selective serotonin reuptake inhibitors
Serotonin and norepinephrine reuptake inhibitors
Suicide
Generalized anxiety disorder
Anxiety disorders: Clinical
Social anxiety disorder
Panic disorder
Obsessive-compulsive disorder
Endocrine system anatomy and physiology
Acromegaly
Insulin
Glucagon
Growth hormone deficiency
Hunger and satiety
Wound healing
Anticoagulants: Direct factor inhibitors
Platelet plug formation (primary hemostasis)
Cartilage structure and growth
Oxygen-hemoglobin dissociation curve
Karyotyping
Fluorescence in situ hybridization
Bone histology
Nasal cavity and larynx histology
Adrenal gland histology
Bronchioles and alveoli histology
Cartilage histology
Thyroid and parathyroid gland histology
Pancreas histology
Skeletal muscle histology
Trachea and bronchi histology
Arteriole, venule and capillary histology
Sympathetic nervous system
Parasympathetic nervous system
Nervous system anatomy and physiology
Cholinergic receptors
Muscle contraction
Muscle weakness: Clinical
Skin anatomy and physiology
Psoriasis
Epidermolysis bullosa
Albinism
Vitiligo
Acne vulgaris
Skin cancer
Alopecia areata
Sunburn
Actinic keratosis
Burns
Cell-mediated immunity of CD4 cells
Cell-mediated immunity of natural killer and CD8 cells
Pneumonia
Vaccinations
Introduction to the immune system
Monoclonal antibodies
Antibody classes
B-cell activation, differentiation, and contraction
B-cell development
Body temperature regulation (thermoregulation)
Cluster headache
Tension headache
Migraine
Meningitis
Brain abscess
Hashimoto thyroiditis
Thyroid hormones
Euthyroid sick syndrome
Human development week 2
Human development days 4-7
Human development week 3
Ectoderm
Mesoderm
Endoderm
Adrenal cortical carcinoma
Primary adrenal insufficiency
Congenital adrenal hyperplasia
Adrenocorticotropic hormone
Synthesis of adrenocortical hormones
Ornithine transcarbamylase deficiency
Neuron action potential
Fats and lipids
Innate immune system
T-cell development
Cytokines
T-cell activation
MHC class I and MHC class II molecules
B- and T-cell memory
Graves disease
Asthma
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
Williams syndrome
Calcium pyrophosphate deposition disease (pseudogout)
Osteomalacia
Lipid-lowering medications: Statins
Hyperlipidemia
Blood brain barrier
Cerebrospinal fluid
Guillain-Barre syndrome
Raynaud phenomenon
Myasthenia gravis
Muscular dystrophy
Subarachnoid hemorrhage
Diabetic retinopathy
Hypopituitarism
Hyperpituitarism
Kallmann syndrome
Phosphate, calcium and magnesium homeostasis
Parathyroid hormone
Calcitonin
Vitamin D
Hypercalcemia
Hypocalcemia
Hyperparathyroidism
Hypothyroidism
Hyperthyroidism
Cushing syndrome

Transcript

Watch video only

Albinism, meaning white, is a non-contagious, congenital condition that is defined by a drastic reduction or complete lack of pigmentation in the hair, skin and eyes.

Albinism is often portrayed negatively, like Silas the antagonist in the book “The Da Vinci Code”, which contributes to his diminished quality of life with the disease.

The skin is divided into three layers--the epidermis, dermis, and hypodermis.

The hypodermis is made of fat and connective tissue that anchors the skin to the underlying muscle.

Just above is the dermis, which contains hair follicles, nerves and blood vessels.

And just above, the outermost layer of skin, is the epidermis.

The epidermis itself has multiple cell layers that are mostly keratinocytes - which are named for the keratin protein that they’re filled with.

Keratin is a strong, fibrous protein that allows keratinocytes to protect themselves from getting destroyed when you rub your hands through the sand at the beach.

Keratinocytes start their life at the deepest layer of the epidermis called the stratum basale, or basal layer, which is made of a single layer of small, cuboidal to low columnar stem cells that continually divide and produce new keratinocytes that continue to mature as they migrate up through the epidermal layers.

But the stratum basale also contains another group of cells - melanocytes, which secrete a protein pigment, or coloring substance, called melanin.

Melanin is actually a broad term that constitutes several types of melanin found in people of differing skin color.

These subtypes of melanin range in color from black to reddish yellow and their relative quantity and rate at which they are metabolized define a person’s skin color.

When keratinocytes are exposed to the sun, they send a chemical signal to the melanocytes, which stimulates the melanocytes to produce melanin through a multistep enzymatic reaction that begins with tyrosine.

Once it’s made, the melanocytes move the melanin into small sacs called melanosomes, and these get taken up by newly formed keratinocytes, which will later metabolize the melanin as they migrate into higher layers of the epidermis.

Melanin then acts as a natural sunscreen, because its protein structure dissipates, or scatters, UVB light--which if left unchecked can damage the DNA in the skin cells and lead to skin cancer.

Melanin can also be found at the base of hair follicles to color hair; and in the eyes, including the iris where it contributes to eye color, and the choroid tissue layer of the eye where it helps prevent light reflection.

Albinism is caused by a recessive gene mutation encoding any one of the enzymes needed to produce melanin.

Sources

  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
  4. "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
  5. "Biology and genetics of oculocutaneous albinism and vitiligo – common pigmentation disorders in southern Africa" South African Medical Journal (2013)
  6. "Oculocutaneous albinism" Orphanet Journal of Rare Diseases (2007)