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Microneedling helps increase the absorption of a melanin product into hair follicles, which may improve laser hair removal effectiveness.

A 16-year-old boy had pernicious anemia, autoimmune hemolytic anemia, and later developed alopecia areata.

Segmental vitiligo affects hair follicle melanocytes, causing small, uniform depigmented spots.

Arg1+ macrophages may play a role in Alopecia Areata, offering new treatment targets.

A 90-year-old woman's hand lesion was a rare, aggressive skin cancer treated successfully with surgery.

Dermoscopy helped diagnose a rare skin disease which slightly improved with treatment.

A 13-year-old boy had both lichen planus and vitiligo, suggesting a possible link between the two conditions.

A new mutation in the HR gene causes hair loss in a specific family.

RET mutation is important in familial medullary thyroid carcinoma, and BRAF mutation in papillary thyroid carcinoma is linked to more aggressive cancer and higher death rates.

A newborn girl had a rare case of salivary gland tissue on her chest, which was safely removed.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Treatment with vitamin A did not improve the child's skin condition.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

VESALT improves alopecia areata assessment by including non-scalp areas and is reliable and user-friendly.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

Basal cell carcinoma cases are rising globally.

Surgical removal of a scalp keratoacanthoma is effective and prevents recurrence, but hair may not regrow.

Hair follicles can be used to easily create neurons and glial cells for potential nerve repair.

The new microneedle system improves hair growth in alopecia treatment.

Thorough clinical examination is crucial for diagnosing unusual alopecia.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

A Nigerian baby with neonatal lupus got better with treatment by 6 months.

Tiny particles from brain cells help hair grow by targeting a specific hair growth pathway.

Extraction videodermoscopy is an effective, non-invasive diagnostic tool for eruptive vellus hair cysts.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

A young Caucasian girl had both woolly hair and alopecia areata, which is rare.

Taking photos of your own skin can lead to fewer skin biopsies for mole monitoring.