English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

systemic neurocutaneous genetic condition with an incidence of almost 1 in 6000 to 10000 live births.1 It is autosomal dominant inheritance and approximately two-thirds of the cases occur with spontaneous mutation. The clinical presentation caused by dysfunction of hamartin and tuberin proteins that are products of TSC1 and TSC2 genes is quite variable. The disease is characterized by hamartomas affecting multiple organs, including skin, brain, heart, kidney, lungs and eye.2

Retinal Astrocytoma in a 6-year-old Girl with Tuberous Sclerosis Complex