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The patient was informed that the fetus had died inside her in 1948, but she did not remove it earlier because she lacked the money. [32] Unknown (82) Bogota, Colombia 1973 2013; not extracted (40 years) Patient originally thought to be suffering from gastroenteritis but an abdominal radiography discovered a calcified fetus in her abdomen. [33 ...
Fetus in fetu (or foetus in foetu) is a rare developmental abnormality in which a mass of tissue resembling a fetus forms inside the body of its twin. An early example of the phenomenon was described in 1808 by George William Young. [1] There are two hypotheses for the origin of a fetus in fetu.
In 2009, a 92-year-old woman in China delivered a fetus she'd been carrying for 60 years. In 2008, a 9-year-old girl in Greece was diagnosed with a tumor that turned out to be the undeveloped ...
A bizarre discovery at a hospital in Brazil: Doctors found a 44-year-old fetus inside an 84-year-old woman. The woman went to the hospital complaining of severe stomach pains and dizziness. X-rays ...
The baby boy was stated to be in critical condition then. The deceased mother's body was found on the property on May 15. [61] The boy, named Yovanny Jadiel Lopez, died several weeks later from brain damage. [62] 46-year-old Clarisa Figueroa and her daughter, 29-year-old Desiree Figueroa, were charged with first degree murder among other counts ...
Primary familial brain calcification [1] (PFBC), also known as familial idiopathic basal ganglia calcification (FIBGC) and Fahr's disease, [1] is a rare, [2] genetically dominant or recessive, inherited neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement.
In some situations, the biological ages were up to 30 years off, which is kind of a big deal. The findings highlight “the need for careful consideration of tissue type when estimating epigenetic ...
Generalized arterial calcification of infancy (GACI) is an extremely rare [2] genetic disorder. It is caused by mutations in the ENPP1 gene in 75% of the subjects [ 3 ] or in mutations in the ABCC6 genes in 10% of patients. [ 4 ]