Debris floats in the water at the scene where a helicopter crashed into the Hudson River, Thursday, April 10, 2025, in Jersey City, N.J. (AP Photo/Ted Shaffrey)
The State Department said it does not “discuss the details of our diplomatic communications with other governments.”The Tripoli-based government of Prime Minister Abdul Hamid Dbeibah said in a statement Wednesday that there was “no deal or coordination” with the U.S. to receive migrants. However, it said “some parallel parties” could have agreed to receive them.
That appears to refer to its rival administration in east Libya, which is controlled by powerful military commander Khalifa Hifter. Libya has been split for years between rival administrations in the east and west, each backed by armed groups and foreign governments.The Hifter-led Libya National Army, which controls eastern and southern Libya, also released a statement, denying any deal or understanding to receive migrants from the U.S.“There won’t be any acceptance or reception of them (the migrants) on the territories secured by the Libyan Armed Forces whatever the reasons and justifications are,” it said.
Abuses against migrants in detention in Libya have been widely documented, with U.N. investigators saying they had, including accounts of murder, torture, enslavement, extrajudicial killings and rape.
about repeated beatings and torture while ransoms were demanded of their families. Their bodies showed traces of old and recent injuries, and signs of bullet and knife wounds on their backs, legs, arms and faces.
Magdy reported from Cairo. AP writers Lolita C. Baldor and Seung Min Kim in Washington and John O’Connor in Springfield, Illinois, contributed to this report., most of them caused by a misstep hidden within their genes. Some conditions can be caught early and treated—but in parts of Africa where population data and resources are scarce, many people go undiagnosed. Rodriguez is trying to change that by connecting patients with genetic testing and medical support, while gathering key data from those patients and their families.
“Most rare disease data has been collected from people of European ancestry, so we have very little knowledge about what’s happening in other parts of the world, mainly in Africa,” Rodriguez said.Ndeye Lam looks at photos of her deceased daughter Mariama who died at age 13 of a rare genetic disease, in Dakar, Senegal, Saturday, Jan. 11, 2025. (AP Photo/Annika Hammerschlag)
Ndeye Lam looks at photos of her deceased daughter Mariama who died at age 13 of a rare genetic disease, in Dakar, Senegal, Saturday, Jan. 11, 2025. (AP Photo/Annika Hammerschlag)His research is funded by organizations including the La Caixa Foundation in Spain and the National Ataxia Foundation in the United States. And he has consulted with scientists in China, France, Boston, and elsewhere around the world, documenting rare diseases and novel disease-causing gene variants.