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The hydrogel helps reduce scarring and improve wound healing by releasing salvianolic acid B in acidic conditions.

The new hydrogel is good for wound dressing because it absorbs water quickly, has high porosity, can release drugs, fights bacteria, and helps wounds heal with less scarring.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.

An 18-year-old girl with pemphigus vulgaris needed strong medication and careful treatment due to ineffective initial therapies and side effects.

A 9-year-old girl developed type 1 diabetes and alopecia after being treated for a rare kidney disease.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

Lichen planus commonly affects middle-aged adults, often involves limbs and mucosal areas, and can be linked to immune diseases.

Unique fat cells near fibrotic areas contribute to systemic sclerosis progression.

MSC-CM improved aged skin in mice.

Recognizing unusual symptoms in Crohn's disease is crucial for proper treatment.

A woman developed a persistent skin rash and hair loss from a condition linked to her increased L-tryptophan intake.

Notch signaling disruptions can cause various skin diseases.

People with Down syndrome have a higher risk of skin disorders and need better screening and treatment.

A new carrier improves skin delivery of tofacitinib for treating inflammatory skin diseases.

Children with HIV often have skin problems that can indicate the severity of their immune system damage.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

Early diagnosis and prednisone treatment can improve outcomes in Cronkhite-Canada syndrome.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

Mutations in keratin genes cause skin disorders, but new treatments show promise.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.