Homozygous acute intermittent porphyria (Q96982)
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The clinical pictures of a case of homozygous acute intermittent porphyria were characterised by porencephaly and severe retardation in development.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1977383835 |
||
| English | Homozygous acute intermittent porphyria |
The clinical pictures of a case of homozygous acute intermittent porphyria were characterised by porencephaly and severe retardation in development. |
Statements
CID11:ID_1977383835
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dki-india-ID_1977383835
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Concluído
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15 August 2026
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