ALAD porphyria (Q97018): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
A porfiria por deficiência de ALA desidratase é uma forma extremamente rara de porfiria hepática aguda caracterizada por ataques neuro-viscerais sem manifestações cutâneas. A doença ocorre em crianças. Os pacientes sofrem ataques neuro-viscerais agudos, que persistem por várias semanas e se manifestam como dor abdominal intensa e sintomas neurológicos e psicológicos. | |||
| description / en | description / en | ||
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. | |||
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 |
||
| 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. |
