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A rare skin condition was found in a Labrador retriever outside North America.

Hair shaft changes may be linked to CCCA, but their role is unclear.

Trichoscopic examination is crucial for diagnosing congenital triangular alopecia.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

A girl's severely tangled hair couldn't be fixed and had to be cut due to a rare condition called plica neuropathica.

A 17-year-old girl with Kartagener's syndrome also has unusual skin, hair, and nail issues.

The case suggests that dissecting cellulitis of the scalp can occur in a White child and should be considered when diagnosing pediatric scarring alopecia.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

LC-OCT helps accurately diagnose different types of infant hair loss without invasive methods.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

The analyses helped identify different skin diseases in the two dogs.

The meeting showcased rare skin disease cases, highlighting the need for accurate diagnosis and treatment.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Dissecting cellulitis may have genetic links and can cause permanent hair loss.

Dermoscopy can help diagnose tinea capitis in children by looking for comma hairs, black dots, and broken hairs with white bands.

A 19-year-old man had a rare skin condition on one side of his face that looked like another skin disease.

Sphynx cats have abnormal hair follicles and keratinization affecting their skin.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Netherton Syndrome can cause severe skin lesions in rare cases.

Shiny white structures in trichoscopy can indicate long-standing discoid lupus erythematosus alopecia.

Plaque-type herpetic folliculitis affects eccrine glands.

A baby with a rare metabolic disorder developed a rash not cured by zinc alone, likely due to both zinc and amino acid deficiencies.

LC-OCT is a useful noninvasive tool for diagnosing and monitoring alopecia areata.

A girl had two rare hair conditions that helped understand their overlap.

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

Yellow dots look different in various hair loss conditions and can help diagnose them.