Congenital glucose-galactose malabsorption due to SLC5A1 mutation: a case of hypernatraemic dehydration
Congenital glucose-galactose malabsorption (GGM) is an exceedingly uncommon autosomal recessive metabolic state defined by persistent diarrhoea along with serious dehydration. It is a disease that is difficult to consider in differential diagnosis and may be fatal if left untreated. This report det...
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| Autori principali: | , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Pakistan Medical Association
2026-03-01
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| Serie: | Journal of the Pakistan Medical Association |
| Soggetti: | |
| Accesso online: | https://jpma.org.pk/index.php/public_html/article/view/22994 |
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