Congenital enterocyte heparan sulphate deficiency (Q100069): Difference between revisions
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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 |
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| 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. |
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CID11:ID_506034123
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dki-india-ID_506034123
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