Prince Fredrick of Luxembourg died 22 years old at the age of 22, a rare genetic disorder, with which he was born, said his family.

Frederic de Nassown died in Paris on March 1, one day after the day of the rare international illness, which is held on the last day of February, Luxembourg. Citizen Website: Prince Frederick founded the organization in 2021 to help raise awareness about the condition.

Prince Robert; His wife, Princess Julie, Princess of Nasau. And all of them, Alexander Frederic's sisters, were able to say goodbye to him on the last day, said the patriarch. One of the last things, Frederick asked him, “Papa, you are proud for me.” According to Prince Robert.

“He was hardly able to talk for a few days, so the clarity of these words was amazing as the weight of the moment was deep,” Ishkhan Robert wrote. “The answer was very easy, and he had heard many times. But at the moment, he needed to assure him that he could have in his short and beautiful existence.

The young prince remembers as a happy man, a “insufficient desire to life.” He was a big fan of Adjusting the “office” in Italian and the USA, which he had completely seen 10 times more than 10 times, said Prince Robert.

What is Polg Mitochondrial disease?

Polg is the gene name that gives instructions to make an active piece called Alpha Subunit, POLYMERASE GAMMA National Medicine of MedicineA number

There are many polg diseases and conditions, including Alpers-Huttenlocher syndrome, ataxia neurology Spectrum and childhood Myocerepropepatopathy spectrum.

Frederic was born in Poli's disease, but he was not diagnosed until he was 14 years old, said his father.

According to PolG Foundation, Frederik's Mitochondrial Disorder “looted body energy cells” and could cause a number of symptoms, including progressive dysfunction and many organs.

“It can be compared to having a faulty battery, which is never fully charging, is in permanent condition, and eventually loses power.

According to experts, about 2% of the population is of PolG mutations. However, the total number of people with polg diseases is unknown. One teaching PolG mutations with adult adults in Australia found that 10% of them had diseases related to Polg.