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Cronkhite-Canada syndrome is a rare disorder needing early recognition and treatment with immunosuppressive therapies and nutritional support to manage symptoms and prevent complications.

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A baby girl had two brain-related growths removed and is developing normally.

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A simple enrichment program improves health and reproduction in Calomys callosus.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Online medical education helps doctors better understand and treat nail fungus.

CLASI is a valid tool for assessing skin activity and damage in lupus patients.

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Managing rare genetic diseases like osteogenesis imperfecta and Escobar syndrome is complex and requires both medical and surgical treatments.

Recognizing RSCC is crucial due to its aggressive nature and high risk of poor outcomes.

Bruce Lee's martial arts philosophy can guide personal development in Plastic & Reconstructive Surgery.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

Short-chain fatty acids from *Cutibacterium acnes* cause skin inflammation, contributing to acne.

Gap junctions help control feather pattern formation in chickens.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

The Core Curriculum for Hair Restoration Surgery aims to improve doctor training for better, safer, and more natural-looking hair loss treatments.

A multidisciplinary approach is crucial for managing Silver-Russell syndrome effectively.

Collider bias can distort our understanding of COVID-19 risk and severity.

Geranium Sibiricum L extract may promote hair growth by increasing growth factors and decreasing inhibitory factors under stress.

Jojoba oil is beneficial for skin, hair, and health but has economic challenges for large-scale farming.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A Korean baby with nevus sebaceus syndrome was found to have a KRAS gene mutation.