ALAD porphyria (Q97018): Difference between revisions
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15 August 2026
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Latest revision as of 13:03, 16 August 2026
Porphyria due to ALA dehydratase deficiency, also called Porphyria of doss, is an extremely rare form of acute hepatic porphyria characterised by neuro-visceral attacks without cutaneous manifestations. The disease occurs in children. Patients suffer acute neuro-visceral attacks, which persist for several weeks and manifest as intense abdominal pain, and neurological and psychological symptoms.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1158153414 |
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| English | ALAD porphyria |
Porphyria due to ALA dehydratase deficiency, also called Porphyria of doss, is an extremely rare form of acute hepatic porphyria characterised by neuro-visceral attacks without cutaneous manifestations. The disease occurs in children. Patients suffer acute neuro-visceral attacks, which persist for several weeks and manifest as intense abdominal pain, and neurological and psychological symptoms. |
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CID11:ID_1158153414
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dki-india-ID_1158153414
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Concluído
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15 August 2026
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