Results 41 to 50 of about 4,220 (193)
Fulminant Wegener's granulomatosis: A case report [PDF]
Introduction. Granulomatosis Wegener is anti-neutrophil cytoplasmic antibodies (ANCAs)-associated systemic vasculitis of unknown etiology. It is manifested as granulomatous necrotizing inflammation of the upper and lower parts of the respiratory tract,
Dinić Miroslav Ž. +3 more
core +1 more source
Necrotizing Fasciitis of Eyelid in Children: A Rare Complication of Varicella Infection
ABSTRACT Necrotizing fasciitis (NF) of the eyelid is an extremely rare but severe complication of varicella zoster virus (VZV) infection in children. We present a case of an 8‐year‐old girl who developed necrotizing fasciitis of the left eyelid following varicella infection.
Govinda Bhandari +2 more
wiley +1 more source
Protein C is an anticoagulant that is encoded by the PROC gene. Protein C deficiency (PCD) is inherited in an autosomal dominant or recessive pattern.
Mariam S. Al Harbi, Ayman W. El-Hattab
doaj +1 more source
Thigh echymosis in a newborn [PDF]
Background and aim: Protein C is one of the important components in haemostasis system and its deficiency could increase the risk of thromboembolic events. This deficiency is seen in 0.2% of the general population.
Alaee, E., Zahedpasha, Y.
core
Blood coagulation from the beginning until to-day [PDF]
The authors give an account of the important developments in blood coagulation knowledge from the times of Malpighi and Moravitz to data. The article is followed by original tables providing a general and comprehensive view on blood coagulation ...
Szirmai, Endre
core +1 more source
Neisseria meningitidis-induced acute systemic meningococcal disease is an emergency and a fatal condition that has a high mortality rate. In patients with a fulminant infection, a maculopapular petechial eruption, purpura fulminans, or an ecchymotic ...
Meng-Yu Wu +5 more
doaj +1 more source
Mutilations Due to Medical Disorders in Children [PDF]
Soft-tissue and bone necrosis, although rare in childhood, occasionally occur in the course of infectious diseases, either viral or bacterial, and seem to be the result of hypoperfusion on a background of disseminated intravascular coagulation ...
Leal, MJ, Palácios, J, Serafim, Z
core
Inherited thrombophilia in pediatric venous thromboembolic disease: Why and who to test [PDF]
Venous thromboembolic disease in childhood is a multifactorial disease. Risk factors include acquired clinical risk factors such as a central venous catheter and underlying disease and inherited thrombophilia.
Nowak-Göttl, U. (Ulrike) +1 more
core +2 more sources
Thrombosis in Brothers With Protein S Deficiency: Case Series
ABSTRACT Hereditary protein S deficiency is a rare thrombophilia that increases the risk of venous thromboembolism (VTE), including thrombosis in unusual sites. Early diagnosis, familial screening, and long‐term anticoagulation are essential for preventing complications and improving outcomes.
Abate Bane Shewaye +5 more
wiley +1 more source

