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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.

A woman with Castleman's disease died from respiratory failure due to bronchiolitis obliterans.

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.

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

It's important to understand the differences between FMF and PFM in children.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

Recognizing bamboo hair helps diagnose Netherton’s syndrome.

A woman with a rare type of dermatomyositis improved with low-dose prednisone and methotrexate.

A clinically suspected melanoma appeared benign under the microscope but was confirmed by specific tests and a rare mutation.

New microneedle method improves hair regrowth treatment delivery.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

Prurigo nodularis is hard to diagnose and treat, but new biologics offer hope for better management.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

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

AKN might be a skin marker for metabolic syndrome.

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