Meital Ben Ari, a co-founder of “Freedom Farm” pats Gary, a sheep with leg braces, at the farm which serves as a refuge for mostly disabled animals in Moshav Olesh, Israel on March 7, 2019. (Photo by Nir Elias/Reuters)

Relatives of the victims, died in the Israeli airstrikes, mourn as they take the bodies from the morgue of Nasser Hospital for the funeral ceremony as the Israeli army attacks continue in Khan Yunis, Gaza on November 14, 2023. (Photo by Belal Khaled/Anadolu via Getty Images)

A one-horned rhinoceros crosses a road inside Kaziranga national park on the eve of the World Rhino Day in Gauhati, India, Tuesday, September 21, 2021. Kaziranga is home to nearly 2,500 one-horned rhinos and is the world’s largest habitat for the rare animal. (Photo by Anupam Nath/AP Photo)

Migrants seeking asylum in the U.S., who returned to the Mexican side of the border to avoid deportation, play soccer in a makeshift migrant camp in Braulio Fernandez Ecological Park in Ciudad Acuna, Mexico, September 22, 2021. (Photo by Go Nakamura/Reuters)

Turkey's Yamaha rider Toprak Razgatlioglu celebrates winning the world championship during the World Superbike Championship at the Mandalika International Circuit in Kuta Mandalika, in central Lombok on November 21, 2021. (Photo by Bay Ismoyo/AFP Photo)

A snow leopard looks on from an inside of a cage, after being captured from the southern plains of Nepal and brought to the central zoo, which wildlife experts say is rare for the animal that is found in the higher altitude, in Kathmandu, Nepal on January 26, 2024. (Photo by Navesh Chitrakar/Reuters)

French twins Thomas and Vincent (L) Seris take the tram in Bordeaux, November 12, 2014. Born with Xeroderma Pigmentosum (XP), the twins cannot be exposed to the sun and its ultraviolet (UV) light, which could provoke precocious cancers due to an autosomal recessive genetic disorder of DNA repair. Colloquially referred to as Children of the Night (Les Enfants de la Lune) the Seris twins are among 70 to 80 people in France who suffer from the genetic defect. The French association “Les Enfants de la Lune” reports that there are between five and ten thousand such cases in the world. Thomas and Vincent have been testing a new protective mask for the last year which is transparent and ventilated and developed by several hospitals in France. (Photo by Regis Duvignau/Reuters)

“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)