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A more sensitive assay was developed to detect enzyme activity converting arginine to citrulline in hair follicles.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Hair transplants can effectively treat hair loss from CCCA in African American women if there's no inflammation.

Radiation therapy with chemotherapy can cause severe, long-lasting hair loss.

Ultrasound effectively distinguishes trichilemmal cysts from epidermoid cysts.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Ivacaftor can protect against noise-induced hearing loss by reducing oxidative stress.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Hair follicle stem cells may help treat strokes.

The method shows how hair lipids form specific patterns and their roles in hair structure.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Whole hair strands can reliably measure gamma ray exposure using ESR techniques, but samples should be analyzed quickly or stored in liquid nitrogen.

A woman with HIV had a severe skin condition that improved with antiretroviral therapy.

Different types of PCOS in Chinese Han women show varying levels of male hormone and metabolic issues.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

Trichoepithelioma and desmoplastic trichoepithelioma have distinct features that can be identified using reflectance confocal microscopy.

Most rural children with scalp ringworm had a non-inflammatory type and early treatment is important to prevent complications.

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

Trichoscopy is important for planning treatment of hair loss after burns.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

Early diagnosis and treatment of NCCAH can improve symptoms and fertility.

Providing housing and case management reduces hospital visits for chronically ill homeless adults.

A new genetic mutation was found causing hair and eye issues in a boy.

Trichoscopy is essential for early detection and monitoring of female-pattern hair loss.

High-frequency ultrasound effectively evaluates and diagnoses frontal fibrosing alopecia.

Ritlecitinib shows promise for treating alopecia areata, especially with early and extended treatment.

Treat limited stage small cell lung cancer with chemotherapy and radiation, and consider preventive brain radiation for better survival chances.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

Proximal hair cortisol is a reliable tool for diagnosing Cushing's Syndrome.