FG syndrome
FG syndrome noun: a rare genetic disorder linked to the X chromosome, causing physical anomalies and developmental delays, characterised by retardation, hyperactive behaviour, constipation, hypotonia, and a characteristic facial appearance.
Noun
FG syndrome (uncountable)
- A rare genetic disorder linked to the X chromosome, causing physical anomalies and developmental delays, characterised by retardation, hyperactive behaviour, constipation, hypotonia, and a characteristic facial appearance.
- Synonyms:
- Opitz-Kaveggia syndrome
Synonyms of FG syndrome
Origin of FG syndrome
From the initials of the surnames of two sisters who had five sons with the syndrome.
Questions about FG syndrome
- What does FG syndrome mean?
- FG syndrome means a rare genetic disorder linked to the X chromosome, causing physical anomalies and developmental delays, characterised by retardation, hyperactive behaviour, constipation, hypotonia, and a characteristic facial appearance.
- What part of speech is FG syndrome?
- FG syndrome is a noun.
Words near FG syndrome in the dictionary
Source and license
Adapted from Wiktionary: FG syndrome (page history and authors). Text available under the Creative Commons Attribution-ShareAlike 4.0 license. Word.ws reformatted the entry and added links. Wiktionary data of 2026-09-02.
Last updated:
Cite this entry: “FG syndrome.” Word.ws, https://word.ws/fg_syndrome. Based on Wiktionary, CC BY-SA 4.0.
