Cystinosis

30,950views

Cystinosis

HMBP

HMBP

Glycolysis
Citric acid cycle
Electron transport chain and oxidative phosphorylation
Gluconeogenesis
Glycogen metabolism
Pentose phosphate pathway
Physiological changes during exercise
Amino acid metabolism
Nitrogen and urea cycle
Fatty acid synthesis
Fatty acid oxidation
Ketone body metabolism
Cholesterol metabolism
Essential fructosuria
Hereditary fructose intolerance
Galactosemia
Pyruvate dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Lactose intolerance
Glycogen storage disease type I
Glycogen storage disease type II (NORD)
Glycogen storage disease type III
Glycogen storage disease type IV
Glycogen storage disease type V
Leukodystrophy
Metachromatic leukodystrophy (NORD)
Krabbe disease
Gaucher disease (NORD)
Niemann-Pick disease types A and B (NORD)
Niemann-Pick disease type C
Fabry disease (NORD)
Tay-Sachs disease (NORD)
Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD)
Mucopolysaccharide storage disease type 2 (Hunter syndrome) (NORD)
Cystinosis
Hartnup disease
Alkaptonuria
Ornithine transcarbamylase deficiency
Phenylketonuria (NORD)
Cystinuria (NORD)
Homocystinuria
Maple syrup urine disease
Abetalipoproteinemia
Familial hypercholesterolemia
Hypertriglyceridemia
Hyperlipidemia
Disorders of carbohydrate metabolism: Pathology review
Disorders of fatty acid metabolism: Pathology review
Dyslipidemias: Pathology review
Glycogen storage disorders: Pathology review
Lysosomal storage disorders: Pathology review
Disorders of amino acid metabolism: Pathology review
Cellular structure and function
Cell membrane
Selective permeability of the cell membrane
Extracellular matrix
Cell-cell junctions
Endocytosis and exocytosis
Osmosis
Resting membrane potential
Nernst equation
Cytoskeleton and intracellular motility
Cell signaling pathways
Adrenoleukodystrophy (NORD)
Zellweger spectrum disorders (NORD)
Primary ciliary dyskinesia
Alport syndrome
Ehlers-Danlos syndrome
Osteogenesis imperfecta
Marfan syndrome
Vitamin C deficiency
Peroxisomal disorders: Pathology review
Nuclear structure
DNA structure
Transcription of DNA
Translation of mRNA
Gene regulation
Epigenetics
Amino acids and protein folding
Protein structure and synthesis
Nucleotide metabolism
DNA replication
Lac operon
DNA damage and repair
Cell cycle
Mitosis and meiosis
DNA mutations
Lesch-Nyhan syndrome
Orotic aciduria
Adenosine deaminase deficiency
Xeroderma pigmentosum
Li-Fraumeni syndrome
Bloom syndrome
Fanconi anemia
McCune-Albright syndrome
Acute radiation syndrome
Purine and pyrimidine synthesis and metabolism disorders: Pathology review
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
Gel electrophoresis and genetic testing
ELISA (Enzyme-linked immunosorbent assay)
Karyotyping
DNA cloning
Fluorescence in situ hybridization
Mendelian genetics and punnett squares
Hardy-Weinberg equilibrium
Inheritance patterns
Independent assortment of genes and linkage
Evolution and natural selection
Down syndrome (Trisomy 21)
Edwards syndrome (Trisomy 18)
Patau syndrome (Trisomy 13)
Fragile X syndrome
Huntington disease
Myotonic dystrophy
Friedreich ataxia
Turner syndrome
Klinefelter syndrome
Prader-Willi syndrome
Angelman syndrome
Beckwith-Wiedemann syndrome
Cri du chat syndrome
Williams syndrome
Alagille syndrome (NORD)
Achondroplasia
Polycystic kidney disease
Familial adenomatous polyposis
Hereditary spherocytosis
Multiple endocrine neoplasia
Neurofibromatosis
Tuberous sclerosis
von Hippel-Lindau disease
Albinism
Cystic fibrosis
Hemochromatosis
Sickle cell disease (NORD)
Alpha-thalassemia
Beta-thalassemia
Wilson disease
X-linked agammaglobulinemia
Hemophilia
Muscular dystrophy
Wiskott-Aldrich syndrome
Mitochondrial myopathy
Autosomal trisomies: Pathology review
Muscular dystrophies and mitochondrial myopathies: Pathology review
Miscellaneous genetic disorders: Pathology review

Transcript

Watch video only

With cystinosis, “cystin-” refers to cystine, an amino acid, and “-osis” implies disease.

So, cystinosis is a rare condition caused by mutations of the CTNS gene that leads to a cystine buildup in the body.

This can cause tissue damage, especially in the kidneys and eyes.

Cystine is an amino acid that comes from our diet.

When food travels through the stomach and intestines, the proteins within, are broken down into tiny fragments, called oligopeptides, or small strings of amino acids.

Turnover of muscle, bone and other parts of the body provide another source of protein that can be broken down into oligopeptides.

Many of these oligopeptides end up in specialized vesicles, called lysosomes, found inside all of our cells.

Here, they are further broken up into amino acids like cystine.

Now, cystine, like any other amino acid has to leave the lysosome, and it does this with the help of a specific protein.

Generally, genes tell our bodies how to make proteins.

So, the CTNS gene encodes for the protein cystinosin, a transporter that is found embedded in the lysosomal membrane.

It’s function is to export cystine out of the lysosome.

Now, in cystinosis, any one of over 100 mutations can affect the CTNS gene, leading to a defective cystine transporter.

Without a working transporter, cystine has no way of leaving the lysosome, so it accumulates, turning into cystine crystals in the process.

Crystals that slowly damage organs like the kidneys and eyes.

In general, humans have two copies of their genes, so both must be damaged for there to be so little cystine transport that cystinosis occurs.

That means that a person with cystinosis must receive a mutated CTNS gene from both the mother and father.

For each such mating, there is a 25% chance that both parents will pass down their own CTNS mutation to the offspring.

Now, depending on the CTNS gene mutation, three types of cystinosis can develop that differ in the age of onset and severity of symptoms.

They are nephropathic, or infantile, late onset, and ocular.

Key Takeaways

Cystinosis is a rare, progressive genetic disorder caused by a mutation in the CTNS gene, which results in the build-up of cystine amino acid in the body. CTNS gene encodes for cystinosin protein, which transports cystine protein out of lysosomes. When it malfunctions, that's when the amino acid accumulates and causes cystinosis. Symptoms include blindness, kidney failure, and muscle weakness.

Sources

  1. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  2. "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
  3. "Yen & Jaffe's Reproductive Endocrinology" Saunders W.B. (2018)
  4. "Bates' Guide to Physical Examination and History Taking" LWW (2016)
  5. "Robbins Basic Pathology" Elsevier (2017)
  6. "Cystinosis" New England Journal of Medicine (2002)
  7. "The de Toni-Fanconi Syndrome with Cystinosis" A.M.A. Journal of Diseases of Children (1958)
  8. "Lysosomal cystine accumulation promotes mitochondrial depolarization and induction of redox-sensitive genes in human kidney proximal tubular cells" The Journal of Physiology (2016)