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About 2.2% of women with symptoms of high male hormones have a mild form of congenital adrenal hyperplasia, and measuring a specific hormone level can accurately diagnose it.

A rare type of skin lymphoma was identified, affecting hair follicles and sweat glands.

Different S100 proteins have specific roles in various parts of the hair follicle.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

Basonuclin helps identify and track hair follicle development and cycling in mice.

Tanning ability is linked to specific DNA changes in skin genes.

HBCs in the olfactory epithelium can self-renew or differentiate into other cell types, with specific patterns during regeneration.

Calcifying epithelioma cells can differentiate into hair cortex and outer root sheath.

A new method helps identify and classify different types of hair casts.

Increased LC3 gene expression may be linked to premature graying of hair.

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

Hair follicle stem cells can help repair nerve injuries.

A gene mutation in mice causes permanent hair loss and skin issues.

Thorough history and examination are crucial for diagnosing genetic disorders like juvenile polyposis and hypomelanosis of Ito.

Boron neutron capture therapy for head and neck cancer can cause side effects like mouth sores and skin irritation, which vary depending on where the treatment is aimed.

A woman with breast cancer developed a rare condition causing excessive fine hair growth on her face and body.

The study maps how genes are regulated during mouse hair growth.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.

Multiphoton microscopy can effectively detect early endometrial cancer by analyzing collagen changes.

Monilethrix is linked to a gene cluster on chromosome 12.

A 21-year-old male has a benign skin condition called Becker's nevus, which he chose not to treat.

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.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Hairless mice have longer hair follicles and abnormal structures during the catagen phase.

FOXN1 duplication can cause excessive hair growth.

Mast cells may significantly contribute to central centrifugal cicatricial alopecia.

Two cases showed skin abnormalities without bone or neural defects.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.