FG syndrome (Q94172): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/156523187 / rank | |||
Normal rank | |||
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 |
||
| 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. |
