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... severity. Severe hyperbilirubinemia is unusual and hyudrops fetalis extremely rare. The pathophysiology of ABO hemolytic disease is identical to that to Rh disease. The antibody causing the immune destruction is of the lgG class. Since igM anti – A or anti-B cannot cross the placenta. ABO hemolytic ...
Applications that address gaps in knowledge of energy system
Applications that address gaps in knowledge of energy system

... It is now recognized that ME/CFS is a complex disease that has been disenfranchised and misunderstood - even stigmatized for so long. Concordantly, the Institute of Medicine (IOM) was commissioned by several federal agencies including the NIH alongside AHRQ, CDC, FDA, SSA and others to establish cle ...
Croup and Bronchiolitis
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Skin Changes on the Forehead - STA HealthCare Communications
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Autoimmunity and autoinflammation
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... To view the Multimedia News Release, please click here. While the total number of infected individuals is unknown due to a lack of available data, the World Health Organization (WHO) estimates that approximately 150 million people globally are currently living with the blood-borne infectious disease ...
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Behçet's disease



Behçet's disease or Behçet disease (/bɛˈtʃɛt/), sometimes called Behçet's syndrome, Morbus Behçet, Behçet-Adamantiades syndrome, or Silk Road disease, is a rare immune-mediated small-vessel systemic vasculitis that often presents with mucous membrane ulceration and ocular problems. Behçet's disease (BD) was named in 1937 after the Turkish dermatologist Hulusi Behçet, who first described the triple-symptom complex of recurrent oral aphthous ulcers, genital ulcers, and uveitis. As a systemic disease, it can also involve visceral organs such as the gastrointestinal tract, pulmonary, musculoskeletal, cardiovascular and neurological systems. This syndrome can be fatal due to ruptured vascular aneurysms or severe neurological complications.
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