Genet Test Mol Biomarkers
Molecular Diagnosis and Identification of Genetic Variants Underlying Distal Renal Tubular Acidosis in Pakistani Patients Using Whole Exome Sequencing.
Khan N, Akhtar N, Khan FF, Hussain S, Naeem M
Introduction: Primary distal renal tubular acidosis (dRTA) is a rare genetic disorder characterized by an impaired urinary acidification process in di ...
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Source: PubMed
Curr Infect Dis Rep
Acute Infectious Diarrhea and Gastroenteritis in Children.
Florez ID, Niño-Serna LF, Beltrán-Arroyave CP
We aimed to summarize the most current evidence on the main aspects of the diarrheal diseases in children. The following key elements were addressed: ...
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Source: PubMed
Int J Environ Res Public Health
Incidence and Risk Factors for Severe Dehydration in Hospitalized Children in Ujjain, India.
Sharma A, Mathur A, Stålsby Lundborg C, Pathak A
Diarrhoea contributes significantly to the under-five childhood morbidity and mortality worldwide. This cross-sectional study was carried out in a ter ...
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Source: PubMed
Radiol Case Rep
Advanced multimodality neuroimaging of a giant, thrombosed MCA aneurysm complicated by an acute stroke in a pediatric patient.
Orman G, Valand HA, Huisman TAGM
A 17-year-old boy presented to our quaternary hospital because of acute mental status changes following prolonged gastrointestinal illness resulting i ...
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Source: PubMed
Klin Padiatr
Failure to Thrive, Hyponatremia, Hyperkalemia - Differential Diagnostic Reflections of a Rare Genetic Disease.
Tropschuh A, de Potzolli B, Seeliger S
Pseudohypoaldosteronism type I is a rare genetic disease of mineralocorticoid resistance that typically manifests in neonatal age. The patients are di ...
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Source: PubMed
