Congenital enterocyte heparan sulphate deficiency (Q100069): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Deficiência congênita de sulfato de heparano em enterócitos é um transtorno do desenvolvimento da mucosa intestinal caracterizado por perda maciça de proteínas entéricas, diarreia secretora e intolerância à alimentação enteral durante as primeiras semanas de vida. Os estudos histoquímicos revelaram uma ausência completa de sulfato de heparano nos enterócitos.
@@ description / en / description / en @@
+Congenital enterocyte heparan sulphate deficiency is a intestinal mucosa development disorder characterised by massive enteric protein loss, secretory diarrhoea, and intolerance to enteral feeds during the first few weeks of life. Histochemical studies revealed a complete absence of enterocyte heparan sulphate.
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+https://id.who.int/icd/entity/506034123
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+https://pauloleads.com.br/cases-publicos/
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+August 2026Timestamp +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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After 0
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++2026-08-15T00:00:00Z
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@@ Property / Collection date: 15 August 2026 / rank @@
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Latest revision as of 16:45, 16 August 2026

Congenital enterocyte heparan sulphate deficiency is a intestinal mucosa development disorder characterised by massive enteric protein loss, secretory diarrhoea, and intolerance to enteral feeds during the first few weeks of life. Histochemical studies revealed a complete absence of enterocyte heparan sulphate.

Language	Label	Description	Also known as
default for all languages	ID_506034123
English	Congenital enterocyte heparan sulphate deficiency	Congenital enterocyte heparan sulphate deficiency is a intestinal mucosa development disorder characterised by massive enteric protein loss, secretory diarrhoea, and intolerance to enteral feeds during the first few weeks of life. Histochemical studies revealed a complete absence of enterocyte heparan sulphate.