The Siberian-born jewelry designer reimagined 12 major metropolises—including London, New York, Paris, Stockholm, and Hong Kong—as intricate accessories you can wear around your finger

Marcelo Maragni was born in Sao Paulo, Brazil. According to his mother’s idea, he was ment to be an architect in a quest of changing the world. Instead, he preferred to take possession of his father’s camera and learn another craft on his own.

Cecilia Paredes was born in Lima, Peru, and lives and works in San Jose and Philadelphia, United States. Her recent photographic work is a conspicuous exploration of sensual surfaces in which the body is deliberately confused with nature and nature with the body.

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)

146 West End Stars hold a flashmob in support of the non-profit organistation Love 146, which campaigns to end child s*x slavery and exploitation, at Trafalgar Sqaure on April 11, 2011 in London, England. (Photo by Tim Whitby/Getty Images)

Child beauty pageants are a billion-dollar industry in the U.S. While some critics see the pageants as an exploitation of innocents, others—particularly pageant parents—view the competitions as a way for a young talent to enter the entertainment industry.

Tessa Evans was born without nose, a very rare facial anomaly called 'arhinia'. The little girl, who is now 18-months-old, has helped in spreading awareness about her condition across the globe.