Ancient DNA Reveals 12,000-Year-Old Case of Rare Genetic Disorder

Ancient DNA Reveals 12,000-Year-Old Case of Rare Genetic Disorder

Researchers from Sapienza University of Rome and Liège University Hospital Centre analyzed ancient DNA from two prehistoric individuals, Romito 1 and Romito 2, found in a double burial at Grotta del Romito in Calabria, southern Italy. The genetic analysis identified variants associated with a rare inherited growth disorder, marking the earliest known genetic diagnosis in humans, dating back approximately 12,000 years. This diagnosis was made in a prehistoric adolescent, providing new insights into the health and genetics of ancient populations in the region. The findings highlight the potential of ancient DNA analysis to reveal medical conditions in prehistoric times.

Դերակատարներ

Romito 2 Romito 1 Sapienza University of Rome Liège University Hospital Centre

Տեղադրություններ

Grotta del Romito

Հոդվածներ

Փետրվար 17, 2026
2 ընդհանուր
Ancient DNA Cracks 12,000-Year Genetic Disorder Mystery
Ancient DNA Cracks 12,000-Year Genetic Disorder Mystery

Mirage News • 17 Փետ 11:42

Researchers have identified genetic variants associated with a rare inherited growth disorder in two prehistoric individuals from southern Italy, marking the earliest known genetic diagnosis in humans.

Վստահելիություն 90% Մանիպ. 5% Կենտրոն
Ancient DNA solves 12,000-year-old mystery of rare genetic growth disorder
Ancient DNA solves 12,000-year-old mystery of rare genetic growth disorder

ScienceDaily • 17 Փետ 11:26

Genetic analysis of a 12,000-year-old double burial in Italy identifies a rare inherited growth disorder in a prehistoric adolescent, providing the earliest known genetic diagnosis.

Վստահելիություն 90% Մանիպ. 5% Կենտրոն