FG syndrome (Q94172): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed an Item |
||||||||||||||
| (6 intermediate revisions by the same user not shown) | |||||||||||||||
| description / pt-br | description / pt-br | ||||||||||||||
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. | |||||||||||||||
| Property / Canonical URI | |||||||||||||||
| Property / Canonical URI: https://id.who.int/icd/entity/156523187 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:ID_156523187 | |||||||||||||||
| Property / CURIE: CID11:ID_156523187 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_156523187 | |||||||||||||||
| Property / Canary Token: dki-india-ID_156523187 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest 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. |
Statements
CID11:ID_156523187
0 references
dki-india-ID_156523187
0 references
Concluído
0 references
15 August 2026
0 references
