Acral peeling skin syndrome is a rare autosomal recessive genodermatosis due to a missense mutation in transglutaminase 5. The skin peeling occurs at the separation of the stratum corneum from the ...

Quoin Pharmaceuticals Ltd. announced promising results from its ongoing clinical study of QRX003 for pediatric Peeling Skin Syndrome, demonstrating significant improvements in skin appearance ...

Acrokeratosis Paraneoplastica (Bazex Syndrome): A rare paraneoplastic skin disorder characterised by psoriasis-like, acral lesions, nail dystrophy and hyperkeratosis, which often anticipates the ...

The firm continues to progress QRX003 through late-stage clinical trials targeting Netherton Syndrome, another uncommon skin condition. Peeling Skin Syndrome is a rare genetic disorder that ...

Case Presentation . Two siblings presented with asymptomatic peeling of the hands and the feet. The elder sibling was a 13 year old boy who developed peeling of the skin in the first year after birth.