Alagille-watson syndrome due to a notch2 point mutation
An autosomal dominant genetic syndrome caused by mutations in the JAG1 gene. It is characterized by cholestatic jaundice in infancy, hepatosplenomegaly, distinctive facial features (prominent forehead, elongated nose, and pointed chin), cardiac murmurs, bone malformations, and sometimes mild mental retardation.
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X-rays are commonly used in clinical practice to diagnose fractures. Characteristics of the fracture such as the type, deformity & soft tissue / joint involvement are used to guide management. Learn & update your basic radiological approach for “Bone Fractures” & interpretation knowledge & patient care approach with this post.
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F.60yrs. LBA with swelling of legs. 3months.
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Check how quickly can you solve these questions using your clinical knowledge. Solve & get a chance to be the top performer. We are Live Now.
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Check out the answer for Quick Brains quiz.
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