Acrofacial dysostosis, Rodriguez type (Q86228): Difference between revisions
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Disostose acrofacial tipo Rodriguez é uma síndrome de malformação múltipla na qual disostose mandibulofacial e defeitos graves de redução de membros estão associados a malformações complexas de diferentes órgãos e sistemas, especialmente o SNC, trato urogenital, coração e pulmões. | |||
| description / en | description / en | ||
Acrofacial dysostosis Rodriguez type is a multiple malformation syndrome in which mandibulofacial dysostosis and severe limb reduction defects are associated with complex malformations of different organs and systems especially the CNS, urogenital tract, heart, and lungs. | |||
Revision as of 11:35, 15 August 2026
Acrofacial dysostosis Rodriguez type is a multiple malformation syndrome in which mandibulofacial dysostosis and severe limb reduction defects are associated with complex malformations of different organs and systems especially the CNS, urogenital tract, heart, and lungs.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_782595225 |
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| English | Acrofacial dysostosis, Rodriguez type |
Acrofacial dysostosis Rodriguez type is a multiple malformation syndrome in which mandibulofacial dysostosis and severe limb reduction defects are associated with complex malformations of different organs and systems especially the CNS, urogenital tract, heart, and lungs. |
