2q31.1 deletion (Q95871)
From determinar.ia.br - Determine suas informações
2q31.1 microdeletion syndrome is a well-defined and clinically recognisable syndrome characterised by moderate to severe developmental delay, short stature, facial dysmorphism and variable limb defects ranging from monodactylous ectrodactyly, brachydactyly and syndactyly to camptodactyly.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_491362822 |
||
| English | 2q31.1 deletion |
2q31.1 microdeletion syndrome is a well-defined and clinically recognisable syndrome characterised by moderate to severe developmental delay, short stature, facial dysmorphism and variable limb defects ranging from monodactylous ectrodactyly, brachydactyly and syndactyly to camptodactyly. |
