| pubmed-article:21874139 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21874139 | lifeskim:mentions | umls-concept:C0020488 | lld:lifeskim |
| pubmed-article:21874139 | lifeskim:mentions | umls-concept:C1533148 | lld:lifeskim |
| pubmed-article:21874139 | lifeskim:mentions | umls-concept:C2700116 | lld:lifeskim |
| pubmed-article:21874139 | pubmed:dateCreated | 2011-8-29 | lld:pubmed |
| pubmed-article:21874139 | pubmed:abstractText | A 4-year-old severely disabled boy with a congenital myopathy developed profuse diarrhoea with hypernatraemia (plasma Na 157 mmol/l). The initial blood urea, serum creatinine and urine output were within normal limits. Despite corrective measures within a hospital setting, the patient's serum sodium peaked at 202 mmol/l. A high fractional excretion of sodium (FE Na) in the context of dehydration and normal renal function was suggestive of a high sodium load. Subsequent investigations revealed an unusual combination of valproate-induced Fanconi syndrome, nephrogenic diabetes insipidus and excess sodium load. The case illustrates why severe hypernatraemia in children is such a diagnostic challenge. | lld:pubmed |
| pubmed-article:21874139 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21874139 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21874139 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21874139 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21874139 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21874139 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21874139 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21874139 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21874139 | pubmed:status | PubMed-not-MEDLINE | lld:pubmed |
| pubmed-article:21874139 | pubmed:issn | 1757-790X | lld:pubmed |
| pubmed-article:21874139 | pubmed:author | pubmed-author:AliTariqT | lld:pubmed |
| pubmed-article:21874139 | pubmed:author | pubmed-author:CrazeJanetJ | lld:pubmed |
| pubmed-article:21874139 | pubmed:author | pubmed-author:AnandGeethaG | lld:pubmed |
| pubmed-article:21874139 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21874139 | pubmed:volume | 2009 | lld:pubmed |
| pubmed-article:21874139 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21874139 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21874139 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:21874139 | pubmed:articleTitle | An unusual case of extreme hypernatraemia. | lld:pubmed |
| pubmed-article:21874139 | pubmed:affiliation | Oxford Radcliffe NHS Trust, Paediatrics, 23, Nether Durford Close, Oxford OX 7FE, UK. | lld:pubmed |
| pubmed-article:21874139 | pubmed:publicationType | Journal Article | lld:pubmed |
