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1.
Ned Tijdschr Geneeskd ; 158: A7540, 2014.
Article in Dutch | MEDLINE | ID: mdl-25269632

ABSTRACT

A twelve-year-old girl was admitted to the paediatric department with progressive joint problems following a mild trauma. Diagnostic follow-up showed a Staphylococcus aureus infection. Generally, S. aureus infection mainly involves the skin and the nasal mucosa. In some cases it can cause a fulminant invasive infection in previously healthy young patients. If this is the case, it is important to consider PVL (Panton-Valentine-leukocidin)-positive S. aureus and underlying immune deficiencies when performing a differential diagnosis. In addition, it is important to remember that previous trauma can cause increased susceptibility to septic arthritis or osteomyelitis in children, as is seen in this case. Aggressive treatment of an invasive S. aureus infection is important even in apparently healthy young patients, to prevent morbidity or mortality.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Arthritis, Infectious/diagnosis , Staphylococcal Infections/diagnosis , Staphylococcus aureus/drug effects , Arthritis, Infectious/drug therapy , Bacterial Toxins/biosynthesis , Bacterial Toxins/toxicity , Child , Diagnosis, Differential , Exotoxins/biosynthesis , Exotoxins/toxicity , Female , Humans , Leukocidins/biosynthesis , Leukocidins/toxicity , Osteomyelitis/diagnosis , Staphylococcal Infections/drug therapy , Staphylococcal Infections/metabolism
2.
JIMD Rep ; 17: 41-6, 2014.
Article in English | MEDLINE | ID: mdl-25086875

ABSTRACT

Decreased bone mass is frequently encountered in classic galactosemia, an inborn error of galactose metabolism. This decrease is most prominent in adults, but is already seen in prepubertal children with increased risk of osteoporosis and fractures later in life. Therefore, bone health in patients with classic galactosemia is increasingly monitored. Although the pathophysiological mechanism is still not fully understood, several factors could negatively affect bone metabolism in this disease. Patients are at risk of nutritional deficiencies due to the galactose-restricted diet. Primary ovarian insufficiency (POI) in female patients also contributes to decreased bone mass. Furthermore, patients with classic galactosemia might be less physically active due to motor or neurological impairments. A disease-specific intrinsic abnormality has been suggested as well. This revised proposal is an update of the 2007 recommendations. In this current approach, we advise comprehensive dietary evaluation, optimization of calcium intake if needed, monitoring and if necessary supplementation of vitamin D, hormonal status evaluation and hormone replacement therapy (HRT) consideration, as well as a regular exercise and assessment of skeletal deformities and clinically significant fractures. We propose bone mineral density (BMD) assessment by serial DXA scans of the lumbar spine, femoral neck, and total hip in adults and lumbar spine and total body less head (TBLH) in children.

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