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Viral reactivation is rare at the time of DRESS diagnosis in the U.S.

Some skin growths with mucin can form hair follicles and resemble skin cancer, but a special stain can help tell them apart.

MC1R gene variations affect skin, hair color, UV sensitivity, and melanoma risk.

Twins had rare skin cysts likely due to genetics.

Early diagnosis and tailored treatment improve outcomes for non-nutritional rickets.

Expanded CD8+ T cells are linked to Alopecia Areata and may cause relapse after treatment.

Macular alopecia is a distinct, non-scarring hair loss pattern that mostly affects young Hispanic/Latinx females and often resolves on its own.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

Monilethrix causes different levels of hair loss in family members.

Reflectance confocal microscopy is a promising non-invasive tool for diagnosing alopecia areata incognita.

A 10-year-old boy recovered from a scalp infection caused by a fungus after treatment with itraconazole.

Tigers had a skin condition causing hair loss and inflammation, but the cause is unknown and treatment didn't work.

Idiopathic hirsutism is the most common cause of hirsutism in women, followed by PCOS.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

CCCA is a hair loss type affecting African women, possibly caused by grooming and chemicals, with various treatments and needing more research.

Reflectance confocal microscopy helped diagnose and manage a woman's hair loss without needing a biopsy.

A 7-year-old girl was diagnosed with Netherton's Syndrome, shown by skin and hair symptoms.

A 9-year-old girl has a rare hair disorder causing beaded, sparse hair.

Ritlecitinib may cause severe musculoskeletal pain in some alopecia universalis patients.

The tumor on the man's nose was a rare type called pedunculated follicular hamartoma.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

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.

Ritlecitinib is effective for treating alopecia areata, showing significant hair regrowth with mild side effects.

CCCA is a scarring hair disorder mainly affecting people of African descent, needing better awareness and treatment.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

A 15-year-old boy was correctly diagnosed with a rare skin condition after initially being misdiagnosed.