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Some skin lymphomas can look like common skin issues and need careful testing to diagnose correctly.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

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

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

A man with hair loss and a scalp lump was diagnosed with a diffuse neurofibroma but chose not to have surgery.

Three genes linked to the development of trichilemmal cysts were found.

Nevoid basal cell carcinomas start in the skin's top layer and hair follicles.

Different growth patterns in thyroid tumors are influenced by where cell growth and death occur.

Spontaneous keloids may be linked to nephrogenic systemic fibrosis in dialysis patients.

A unique skin cell similar to hair bulb melanocytes was identified, with better preservation using permanganate fixation.

Trichoscopy is a helpful tool for diagnosing Netherton syndrome.

A 30-year-old man with rare skin conditions improved with antibiotics and surgery, hinting at a link to rosacea.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Machine learning identified three unique subtypes of androgen excess in women with PCOS, each with different metabolic risks.

Majocchi's granuloma can occur in kidney transplant patients on tacrolimus and can be treated with antifungal medication.

Microneedling with 5% minoxidil improves hair loss in Chinese men by activating Wnt/ß-catenin pathway.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Intralesional steroids effectively treated a young female's scalp nodules without recurrence.

Different ethnic hair types have unique nanoscopic and molecular features despite having the same basic keratin structure.

Syringomas likely start in the upper dermis and form distinct luminal structures.

A genetic variant linked to hair thinning in Japanese women was found.

The human scalp hair bulb contains different types of melanocytes with varying abilities to produce melanin.

Renal transplant patients on tacrolimus and sirolimus may develop acne keloidalis nuchae.

Microneedles with traditional Chinese medicine can help regrow hair in androgenic alopecia.

A rare benign skin growth called melanocytic matricoma was identified in a 69-year-old man.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.