17q11 deletion (Q105756): Difference between revisions
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A síndrome de microdeleção 17q11 é uma forma rara e grave de neurofibromatose tipo 1, caracterizada por leve dismorfismo facial, atraso no desenvolvimento, déficit intelectual e grande número de neurofibromas. | |||
| description / en | description / en | ||
17q11 microdeletion syndrome is a rare severe form of neurofibromatosis type 1, characterised by mild facial dysmorphism, developmental delay, intellectual deficit, and large number of neurofibromas. | |||
Revision as of 12:12, 17 August 2026
17q11 microdeletion syndrome is a rare severe form of neurofibromatosis type 1, characterised by mild facial dysmorphism, developmental delay, intellectual deficit, and large number of neurofibromas.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_919770752 |
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| English | 17q11 deletion |
17q11 microdeletion syndrome is a rare severe form of neurofibromatosis type 1, characterised by mild facial dysmorphism, developmental delay, intellectual deficit, and large number of neurofibromas. |
