FG syndrome
Disease
FG syndrome (FGS) is a rare genetic syndrome caused by one or more recessive genes located on the X chromosome and causing physical anomalies and developmental delays. FG syndrome was named after the first letters of the surnames of the first patients noted with the disease.
Nº Q530142 ★★★
Rare · History
FG syndrome
Disease
FG syndrome (FGS) is a rare genetic syndrome caused by one or more recessive genes located on the X chromosome and causing physical anomalies and developmental delays. FG syndrome was named after the first letters of the surnames of the first patients noted with the disease.
Last price
—
Floor price
—
7-day median
—
30-day sales
0
30-day range
—
In circulation
0
Price history
median
low – high
sales
No sales in this period
Show table
| Date | median | Low | High | sales |
|---|
Sales history
- Last sale
- —
- 30-day average
- —
- 30-day low
- —
- 30-day high
- —
- Sales 7d
- 0
- Sales 30d
- 0
No sales yet.
Anonymous sales: no buyer or seller shown. Figures count player-to-player sales only.
From Wikipedia
FG syndrome (FGS) is a rare genetic syndrome caused by one or more recessive genes located on the X chromosome and causing physical anomalies and developmental delays. FG syndrome was named after the first letters of the surnames of the first patients noted with the disease. First reported by American geneticists John M. Opitz and Elisabeth G. Kaveggia in 1974, its major clinical features include intellectual disability, hyperactivity, hypotonia (low muscle tone), and a characteristic facial appearance including macrocephaly (an abnormally large head).
Text: Wikipédia, CC BY-SA 4.0. · Image: Wikimedia Commons (Attribution) ·
Related cards
Neotenic complex syndrome
Congenital extreme form of developmental delay and neoteny
Nº Q55624965 ★
XY gonadal dysgenesis
Gonadal dysgenesis that is characterized by a normal 46,XY karyotype along with a progressive loss of germ cells on the developing gonads of an embryo
Nº Q957751 ★★★
Kabuki syndrome
Rare disease
Nº Q1538227 ★★★
Primary familial brain calcification
A rare, genetic neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement
Nº Q1947307 ★★
Gerstmann–Sträussler–Scheinker syndrome
Prion disease characterized by adult onset of memory loss, dementia, ataxia, and pathologic deposition of amyloid-like plaques in the brain
Nº Q383228 ★★★★
Bardet–Biedl syndrome
Ciliopathic human genetic disorder that produces many effects and affects many body systems
Nº Q1678281 ★