FG syndrome (Q94172): Difference between revisions
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Síndrome FG (FGS) é uma anomalia congênita múltipla (ACM) recessiva ligada ao X e síndrome de atraso no desenvolvimento com um padrão psicológico característico (atraso no desenvolvimento da integração sensorial, transtorno de déficit de atenção, autoabsorção e fascinação por brinquedos e objetos mecânicos). Homens são afetados, mas meninas e mulheres portadoras também podem ser afetadas, às vezes mais gravemente do que os homens. | |||
| description / en | description / en | ||
FG syndrome (FGS) is a X-linked recessive multiple congenital anomalies (MCA) and developmental delay syndrome with a characteristic psychological pattern (delayed development of sensory integration, attention deficit disorder, self-absorption and fascinations with mechanical toys and objects). Males are affected, but carrier girls and women may also be affected, sometimes more severely than the males. | |||
Revision as of 09:17, 16 August 2026
FG syndrome (FGS) is a X-linked recessive multiple congenital anomalies (MCA) and developmental delay syndrome with a characteristic psychological pattern (delayed development of sensory integration, attention deficit disorder, self-absorption and fascinations with mechanical toys and objects). Males are affected, but carrier girls and women may also be affected, sometimes more severely than the males.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_156523187 |
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| English | FG syndrome |
FG syndrome (FGS) is a X-linked recessive multiple congenital anomalies (MCA) and developmental delay syndrome with a characteristic psychological pattern (delayed development of sensory integration, attention deficit disorder, self-absorption and fascinations with mechanical toys and objects). Males are affected, but carrier girls and women may also be affected, sometimes more severely than the males. |
