Arthrogryposis multiplex congenita with whistling face (Q85057): Difference between revisions
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Revision as of 10:25, 15 August 2026
Arthrogryposis multiplex congenita with whistling face is an extremely rare disorder characterised in newborns by arthrogryposis multiplex congenita with scarce face expressions (whistling face), severe developmental delay, and central nervous system and autonomous nervous system dysfunction (excessive salivation, temperature instability, apnoea, myoclonic epileptic fits and bradycardia).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_210291070 |
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| English | Arthrogryposis multiplex congenita with whistling face |
Arthrogryposis multiplex congenita with whistling face is an extremely rare disorder characterised in newborns by arthrogryposis multiplex congenita with scarce face expressions (whistling face), severe developmental delay, and central nervous system and autonomous nervous system dysfunction (excessive salivation, temperature instability, apnoea, myoclonic epileptic fits and bradycardia). |
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CID11:ID_210291070
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dki-india-ID_210291070
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