Shprintzen-Goldberg syndrome
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Summary
Shprintzen-Goldberg syndrome is a class of disease[1]. It draws 306 Wikipedia views per month (class of disease category, ranking #613 of 1,968).[2]
Key Facts
- Subclass of: craniosynostosis[3]
- Prevalence: 0.000001[4]
- Genetic association: FBN1[5], SKI[6]
- Age of onset: congenital onset[7], infantile onset[8], neonatal onset[9]
- P14914: D02462[10]
Why It Matters
Shprintzen-Goldberg syndrome has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[11] It is known by 9 alternative names across languages and contexts.[12]