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Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A rare scalp tumor was removed from a 49-year-old woman, with a good outlook if benign but needing careful monitoring if malignant.

An 8-year-old girl had nail and hair issues that improved without specific treatment, but fungal nail infection was hard to cure.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

The man's hair loss and skin papules were diagnosed as atrichia with papular lesions, not alopecia areata universalis.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

Topical immunotherapy with DPCP is most effective for certain alopecia areata types, with success linked to age and disease duration, and influenced by a gene polymorphism.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

HPV6/11 is often found in hair of men with anogenital warts, especially pubic hair, and can lead to recurrent warts.

A new syndrome may link skin, growth, mental, and hair issues.

UV light might cause excessive hair growth by increasing PGE2 in the skin.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

LALPS causes non-scarring hair loss along the Blaschko line, with unique trichoscopic findings.

A man's pubic hair infection was treated by shaving and using antifungal medications.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Early recognition and multidisciplinary management of Whitaker syndrome can improve patient outcomes.

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

Dermoscopic and histopathological features combined can help diagnose Pityriasis versicolor.

Two sisters had a rare hair condition without other usual symptoms.

Trichoscopy helps accurately diagnose temporal triangular alopecia.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

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

COVID-19 vaccination may trigger recurrence of cutaneous T-cell lymphoma in some patients.