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Congenital factor II deficiency

An inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms.

Jaundice

Yellow pigmentation of the skin due to bilirubin, which in turn is the result of increased bilirubin concentration in the bloodstream.

Total: 2

(per page)

PMID (PMCID)
9233981	FEMALE
	Auxiliary liver transplant in fulminant failure.
	Rosenthal P, Roberts JP, Ascher NL, Emond JC. Pediatrics. 1997;100(2):E10.
	Fulminant hepatic failure (FHF) is defined as a syndrome of acute liver failure with the development of hepatic encephalopathy and severe hypoprothrombinemia occurring within 2 months of the onset of symptoms or jaundice in a person without preexisting liver disease.
106783	FEMALE	Adult
	Liver failure with steatonecrosis after jejunoileal bypass: recovery with parenteral nutriton and reanastomosis.
	Baker AL, Elson CO, Jaspan J, Boyer JL. Arch Intern Med. 1979;139(3):289-92.
	Two women, aged 41 and 51 years, developed jaundice, encephalopathy, and hypoprothrombinemia during rapid weight loss four and 12 months after jejunoileal bypass for refractory obesity.