Lesch-Nyhan syndrome

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Lesch-Nyhan syndrome


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Lesch-Nyhan syndrome

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A 28-year-old gravida 2 para 1 woman comes to the obstetrician to discuss her pregnancy. The patient is at 20-weeks of gestion. Using ultrasound, the sex of the fetus is determined to be male. The patient is taking prenatal vitamins and is up to date with prenatal care. Both the patient and her partner are healthy. However, the patient’s first male child was diagnosed with Lesch-Nyhan syndrome. The patient asks the physician about the chances of the fetus being affected. Which of the following is the most appropriate response by the physician?  

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Lesch-Nyhan syndrome p. 35


Lesch-Nyhan syndrome p. 35


Lesch-Nyhan syndrome p. 35

Gout p. 477

Lesch-Nyhan syndrome p. 35


Lesch-Nyhan syndrome p. 35

Lesch-Nyhan syndrome p. 35

inheritance p. 60

labs/findings p. 722

Purines p. 191

in Lesch-Nyhan syndrome p. 35

Uric acid

Lesch-Nyhan syndrome p. 35

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Lesch-Nyhan syndrome is a rare genetic condition which leads to excess uric acid in the blood, and it causes kidney, joint, neurological, and behavioral problems.

Normally, each cell contains both DNA and RNA, and diving deeper, each nucleotide can be broken down into a sugar, a deoxyribose in DNA or a ribose in RNA, one to three phosphate groups, and a nucleobase, which can be either a pyrimidine or a purine.

There are three pyrimidine bases– cytosine, thymine and uracil and two purine bases, adenine and guanine.

So, the name of a ribose-containing, monophosphatic nucleotide, based on guanine, would be guanosine monophosphate, or GMP for short, whereas one based on adenine, would be adenosine monophosphate, or AMP, for short.

Now, there are two ways our cells can make nucleotides - one is to make from scratch, also known as de novo synthesis, and the other is the salvage pathway, which recycles nucleotides that are already semi-degraded.

Let’s focus on the purine salvage pathway.

In the case of GMP, the enzyme purine nucleoside phosphorylase, first removes the ribose and the phosphate from it, turning it into guanine.

Next, another enzyme called guanase removes an amine group turning guanine into xanthine.

Finally, xanthine is oxidized into uric acid by the enzyme xanthine oxidase.

On the other hand, for AMP to become uric acid, first the enzyme AMP deaminase removes an amine group from it, turning it into IMP.

Then purine nucleoside phosphorylase comes in and removes the phosphate and the ribose from IMP, making hypoxanthine.

Hypoxanthine is then oxidized twice by xanthine oxidase - first to become xanthine, and then finally, to uric acid.

Uric acid can then be filtered out of the blood and excreted in the urine.

Now those intermediate molecules in purine degradation, guanine and hypoxanthine, can be restored into fresh new nucleic acids, through what is known as a salvage pathway.

There’s an enzyme called hypoxanthine-guanine phosphoribosyl transferase, or HGPRT for short, which returns ribose and phosphate back to guanine to form GMP, and to hypoxanthine to form IMP.

From there, IMP can become AMP again.

Now, in Lesch-Nyhan syndrome, there’s a mutation in HGPRT gene which is on the X chromosome.

So, Lesch- Nyhan syndrome is an X-linked recessive condition, and it almost exclusively occurs in males, because if they get one mutation they get the disease.

In females, a single mutation makes them a carrier, and two mutations are needed to have the disease.


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