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1.
Arch Pediatr ; 27(8): 509-510, 2020 Nov.
Article in English | MEDLINE | ID: mdl-32933816

ABSTRACT

COVID-19 is a new disease leading to respiratory complications in adults. Children appear to have more modest symptoms than adults. Varicella is often described as a benign disease in the pediatric population. However, patients with varicella and COVID-19 co-infection can develop a more serious respiratory infection. We report the case of an infant who had a co-infection with both viruses that led to pleuropneumonia. The main question in the present case concerns the link between COVID-19 and varicella infection, and the possible modulation in immune response due to the two virus infections.


Subject(s)
Betacoronavirus , Chickenpox/diagnosis , Coinfection/diagnosis , Coronavirus Infections/diagnosis , Pleuropneumonia/diagnosis , Pneumonia, Viral/diagnosis , Betacoronavirus/isolation & purification , COVID-19 , Coinfection/virology , Humans , Infant , Male , Pandemics , Pleuropneumonia/virology , SARS-CoV-2
2.
Joint Bone Spine ; 70(2): 149-53, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12713862

ABSTRACT

Hyperuricemia is a well-known consequence of glucose-6-phosphatase (G6Pase) deficiency, the enzymatic abnormality that characterizes glycogen storage disease (GSD) Type Ia. However, acute gout as the presenting manifestation of GSD Type Ia has been reported in only a few patients. We report a new case in a 17-year-old male evaluated for acute gouty tendinitis in the right Achilles tendon. Blood tests showed chronic acidosis with high levels of uric acid, lactic acid, and cholesterol. A liver enzyme study confirmed the diagnosis of GSD Type Ia. A genetic study showed that the index patient and his sister were composite heterozygotes for the known mutation R83C and the previously unreported mutation M5R. Acute gout in an adolescent with liver enlargement and high blood levels of uric acid and cholesterol should suggest GSD. Demonstration by molecular biology techniques of a mutation in both alleles of the G6Pase gene establishes the diagnosis of GSD Type Ia, obviating the need for a liver biopsy.


Subject(s)
Glycogen Storage Disease Type I/diagnosis , Gout/complications , Tendinopathy/etiology , Adolescent , Female , Glycogen Storage Disease Type I/complications , Glycogen Storage Disease Type I/genetics , Heterozygote , Humans , Male , Mutation
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