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A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

New mutations in the DSG4 gene cause a rare hair condition.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

MRL/MpJ mice heal burns slower with more scarring and less tissue regeneration than BALB/c mice.

JW0061 may be a new treatment for hair loss by promoting hair growth through WNT signaling.

Recognizing rare causes of MASLD is crucial for effective treatment and preventing complications.

MYB83 limits root hair growth and helps plants tolerate nutrient deficiencies.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

DMG-Na may improve blood flow and help hair growth without side effects.

Higher testosterone and dehydroepiandrosterone sulphate levels may help diagnose meibomian gland dysfunction.

Geriatric Julia Creek dunnarts often suffer from reproductive and skin diseases, impacting conservation efforts.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

Early detection and treatment of Menkes disease with copper injections are crucial for better outcomes.

A baby with KID syndrome died from infections and organ failure at 18 months old.

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Palmaris longus muscle absence is uncommon and not linked to gender, hand side, or finger ratio.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Accurate diagnosis of RDEB-mitis in older adults is crucial for proper management without immunosuppressants.

Myotonic dystrophy may be classified as a segmental progeroid disorder.

Desmoglein 3 organization in cell connections changes without calcium, affecting cell adhesion.

Preserving and accessing historical research is crucial for ongoing scientific progress.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

Gsdma3 affects hair growth by controlling Wnt5a, which influences hair cell development.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.