Kabuki syndrome (Q94171): Difference between revisions
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Síndrome de Kabuki (SK) é uma síndrome de anomalia congênita múltipla caracterizada por características faciais típicas, anomalias esqueléticas, incapacidade intelectual leve a moderada e deficiência de crescimento pós-natal. | |||
| description / en | description / en | ||
Kabuki syndrome (KS) is a multiple congenital anomaly syndrome characterised by typical facial features, skeletal anomalies, mild to moderate intellectual disability and postnatal growth deficiency. | |||
Revision as of 09:17, 16 August 2026
Kabuki syndrome (KS) is a multiple congenital anomaly syndrome characterised by typical facial features, skeletal anomalies, mild to moderate intellectual disability and postnatal growth deficiency.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1104246467 |
||
| English | Kabuki syndrome |
Kabuki syndrome (KS) is a multiple congenital anomaly syndrome characterised by typical facial features, skeletal anomalies, mild to moderate intellectual disability and postnatal growth deficiency. |
