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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.


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.


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