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The method can identify minerals in hair from water, and using coconut oil or conditioner can prevent mineral buildup.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

SLE and DM can coexist but are rare and need careful evaluation.

Dissolving microneedles can effectively deliver dutasteride for hair loss treatment.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

Non-drug methods effectively managed agitation in a patient with a heart device, leading to improved mental function.

Exclamation mark hairs suggest early scalp disease, while white dots indicate it's chronic.

Most patients with dermatomyositis had skin rash, itching, and muscle weakness, treated mainly with prednisolone and hydroxychloroquine.

A man developed severe skin reactions after using a treatment for hair loss.

Combining amino acid and stem cell therapy may help manage hepatocutaneous syndrome in dogs.

Patients at dermatology specialist hospitals had lower death and readmission rates but higher treatment costs.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Dermoscopy has improved skin cancer diagnosis and has expanding applications in dermatology, but requires staying updated with new research and techniques.

Deep Brain Stimulation helps manage Parkinson's symptoms when medication isn't enough.

ODAC members faced intense pressure but prioritized scientific evidence in drug approval decisions.

Juvenile dermatomyositis can worsen quickly and needs strong treatment.

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

Mutations in the DSG4 gene cause specific hair and scalp issues.

The formulation with oleic acid may be better for treating male pattern baldness.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

The demineralized bone matrix scaffold is better for cell attachment than the mineralized bone allograft.

Dermoscopy helps diagnose different scalp conditions by showing unique signs for each disorder.

Targeting protein S-palmitoylation could lead to new skin disease treatments.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

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

DNCB is highly effective for treating alopecia areata with minimal long-term side effects.

MARCKSL1 is important for wound healing and could be a target to reduce scarring.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

Early diagnosis and treatment of discoid lupus erythematosus improve outcomes.