Journalists interview a girl, member of the Cryophile amateurs winter swimmers club, after bathing in the ice waters of the Yenisei River, during the celebrations for the upcoming Christmas and New Year, in Krasnoyarsk, Russia, December 23, 2017. (Photo by Ilya Naymushin/Reuters)

A girl attends Friday prayers in front of an army tank in Tahrir Square in Cairo February 18, 2011. Five years ago thousands of protesters took to the streets demanding the end of the 30-year reign of President Mubarak as Egypt became the second country to join the Arab Spring. After weeks of clashes, strikes and protests across Egypt, Mubarak resigned on February 11, 2011. (Photo by Suhaib Salem/Reuters)

Yalena Leuliette, 7, of Greenbelt, Md., throws seeds from a cattail plant up in the air as she plays while visiting the Kenilworth Aquatic Gardens in northeast Washington, on Sunday, August 9, 2015. Leuliette visits the public garden with her parents a few times a year. (Photo by Jacquelyn Martin/AP Photo)

A visitor poses next to Chinese charms and ornaments that are seen on display for sale at a shop in the Chinatown district of Manila on February 7, 2024, ahead of the Lunar New Year of the Dragon which falls on February 10. (Photo by Ted Aljibe/AFP Photo)

Rahma, 19 (L), pictured with her 10-year old brother Fahad on June 21, 2016 in Kano, Nigeria. A teenage girl born without limbs lives her life in a plastic bowl. Rahma Haruna is a bright, happy girl, despite suffering from a mystery condition that stopped her arms and legs developing properly – leaving her practically limbless and in constant pain. The 19-year- old, from Kano, Nigeria, was born a healthy baby but when she turned six months old her growth came to a sudden halt and she stopped hitting key development milestones. Rahma’s family do their best to provide her with a fulfilling life and transport her around the village in a plastic bowl. Rahma said: “They help me a lot. How do they? They give me anything I need”. Rahma died on 25 December 2016. (Photo by Sani Maikatanga/Barcroft Images)

“Cockayne syndrome (also called Weber-Cockayne syndrome, or Neill-Dingwall Syndrome) is a rare autosomal recessive congenital disorder characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), and premature aging. Hearing loss and eye abnormalities (pigmentary retinopathy) are other common features, but problems with any or all of the internal organs are possible. It is associated with a group of disorders called leukodystrophies. The underlying disorder is a defect in a DNA repair mechanism. It is named after English physician Edward Alfred Cockayne (1880–1956)”. – Wikipedia

Photo: Mother of 12-year-old Chinese girl Sun Yangyang suffering from Cockayne syndrome, tends her at the First Affiliated Hospital of Jilin University on November 11, 2006 in Changchun of Jilin Province, China. The disease results in the senile appearance of Yangyang and also causes eyesight, hearing weakness and other problems. Doctors failed to cure the girl... (Photo by China Photos/Getty Images)

A girl wears a face mask to curb the spread of the coronavirus as she attends a prayer ceremony to mark the holiday of “Enkutatash”, the first day of the new year in the Ethiopian calendar, which is traditionally associated with the return of the Queen of Sheba to Ethiopia some 3,000 years ago, at Bole Medhane Alem Ethiopian Orthodox Cathedral in the capital Addis Ababa, Ethiopia Friday, September 11, 2020. (Photo by Mulugeta Ayene/AP Photo)

In this Friday, February 27, 2015 photo, an Israeli high-school senior preparing to join the Israeli military later this year participates in a privately run training camp for military combat fitness near Yakum, central Israel. With a mandatory three-year military service looming after graduation, teenage boys, and increasingly girls too, are gearing up for the draft, getting into shape and trying to improve their chances of acceptance into elite combat units. (Photo by Oded Balilty/AP Photo)