Aardvark’s lead candidate ARD-101 is being investigated in a Phase III study for hyperphagia in Prader-Willi syndrome.

Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are imprinting disorders caused by genetic or epigenetic aberrations of 15q11.2-q13. Their clinical testing is often multitiered; diagnostic ...

What is Zollinger-Ellison syndrome? Zollinger-Ellison syndrome (ZES) is a rare digestive disorder. If you have ZES, you likely have 1 or more tumors in the first part of the small intestine, the ...

They have Prader-Willi syndrome (PWS) – a rare neurodevelopmental and genetic condition where the “switch” in the brain that signals fullness never gets flipped on. PWS occurs when part of ...

The Minnesota Twins face a crucial offseason decision regarding utilityman Willi Castro ... at the top of their depth chart. Castro’s versatility would help them at multiple defensive positions ...

Colette Love makes the Radio 4 Appeal on behalf of the Prader-Willi Syndrome Association UK. The charity runs a phone line for families affected by the condition. Show more Colette Love makes the ...

A pedigree with 14 patients affected with microcornea-cataract (MC) syndrome is described. MC syndrome is very rare and this pedigree is probably the sixth to be reported. Transmission is most likely ...

Some of the pedigree charts relate to Down's Syndrome. Most of the pedigree charts are annotated with dates, family names and coding instructions. Also includes family data. The original material is ...

Prader-Willi syndrome (PWS, OMIM176270) is a rare genetic disorder with recognizable dysmorphic features and multisystemic consequences such as endocrine, neurocognitive and metabolic ones. Although ...

NLRP3-associated autoinflammatory disease (NLRP3-AID) (formerly called cryopyrin-associated periodic syndrome, CAPS), an autosomal dominantly ... and the complete medical records were documented, ...