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A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

Type B material, ground for 8 hours, is the most suitable and compatible for use as a soft tissue filler.

DP and DS cells are different from DF cells in structure and function.

Switching insulin brands caused skin lesions in a diabetic woman, resolved by changing to oral medication.

Consider THPP in patients with muscle weakness and low potassium, as it is often underdiagnosed.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

CD133+ cells are crucial for hair growth.

Polydopamine is promising for personalized medicine and biomedical technology due to its strong adhesion and biocompatibility.

The hydrogel helps heal diabetic wounds by reducing infection and inflammation.

Topical diphencyprone effectively treated a 9-year-old boy's alopecia areata with fewer side effects.

Timely diagnosis and treatment of complex autoimmune diseases like APS2 are crucial to prevent complications and improve life quality.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

A rare scalp condition with hair loss was correctly diagnosed and treated, leading to hair regrowth.

Most patients with anal Pemphigus Vulgaris had repeated episodes but fully recovered with treatment, without long-term problems.

DPCP is more effective than tretinoin gel for treating severe alopecia.

Technique creates 3D cell spheroids for hair-follicle regeneration.

PRP injections are safe but don't significantly improve Peyronie's Disease.

Mechanoreceptors convert physical touch into electrical signals through specialized nerve structures.

Post-steroid panniculitis is now rare because doctors taper steroids more carefully.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

New hair loss subtype found, mimics common baldness.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

Recognizing IPPP is crucial to prevent misdiagnosis and unnecessary treatments.

KID syndrome should be reclassified as an ectodermal dysplasia.

The patient with a misplaced pituitary gland and interrupted pituitary stalk is being treated with hormone replacement.

CI-1033 causes skin lesions in rats, similar to humans, due to EGF receptor inhibition.