Hemophilia B Hemophilia B also called Haemophilia B, Christmas disease or Royal disease is an inherited bleeding disorder that is inherited in X-linked recessive pattern caused by a

Hemophilia A Hemophilia A also called Haemophilia A or Classic Hemophilia is an inherited bleeding disorder that is inherited in X-linked recessive pattern caused by a deficiency in

Hemostasis Hemostasis is the body's way of stopping injured blood vessels from bleeding ((LaPelusa A, Dave HD. Physiology, Hemostasis. . In: StatPearls . Treasure Island

Subgaleal hemorrhage Subgaleal hemorrhage is a rare but potentially lethal bleeding condition in newborns caused by the rupture of emissary veins in the loose connective tissue

Cephalohematoma Cephalohematoma is a collection of blood or hematoma between the scalp and the skull periosteum, located in the subperiosteal space and as such, is contained anatomically to

Rotor syndrome Rotor syndrome also called Rotor type hyperbilirubinemia, is a rare, benign, autosomal recessive inherited genetic disorder characterized by hyperbilirubinemia due to elevated levels of both unconjugated bilirubin

Dubin Johnson syndrome Dubin-Johnson syndrome is a rare autosomal recessive inherited disorder of bilirubin transport that is characterized by buildup of bilirubin in the bloodstream (conjugated hyperbilirubinemia),

What is hyperbilirubinemia Hyperbilirubinemia is a medical condition characterized by elevated levels of bilirubin (an orange-yellow pigment formed in the liver by the breakdown of hemoglobin)

What is carotenemia Carotenemia is the term used for increased beta-carotene levels in the blood and yellow pigmentation of the skin. Strictly speaking, excessive carotene

Crigler Najjar syndrome Crigler-Najjar syndrome is a very rare inherited disorder characterized by a persistent high levels of a toxic substance called unconjugated bilirubin in

Pyruvate kinase deficiency Pyruvate kinase deficiency is an inherited disorder that affects red blood cells, which carry oxygen to the body's tissues. People with pyruvate

ABO incompatibility ABO incompatibility is the most common cause of hemolytic disease of the newborn (HDN) which occurs in 15 to 25% of pregnancies ((Murray