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Trichohyalin is found in non-hair tissues and works with filaggrin in certain skin areas and conditions.

Corkscrew hairs can help diagnose trichotillomania.

Hair shaft disorders are diagnosed through examination and history, with general care and some treatments offering improvement.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

Two sisters with Netherton's syndrome had skin and hair issues, needing special diet and ointments.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Endoscopic forehead and brow lifting safely and consistently improves aged eyebrows, but may have complications.

Hydrocortisone ointment effectively improved eyebrow skin and hair in a 10-year-old.

Lupus erythematosus can mimic alopecia areata, and trichoscopy is key for accurate diagnosis and better patient outcomes.

Inverted follicular keratosis on the eyelid can be cured with surgery and has a great prognosis.

Ulerythema ophryogenes causes hair thinning and inflammation, with limited treatment options.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Early diagnosis of Keratosis pilaris atrophicans faciei can lead to better, personalized treatments.

Fractional CO₂ laser treatments effectively tighten eyelid skin and elevate eyebrows safely.

Lykoi cats' unique sparse hair is linked to specific genetic variants in the Hairless gene.

The hair defect is due to abnormal inner root sheath keratinization.

Rectangular black granules, solitary yellow dots, and mostly single-hair follicles suggest Loose Anagen Hair Syndrome.

Trichoscopy can reveal specific hair and scalp changes in linear morphea.

Recognizing bamboo hair helps diagnose Netherton’s syndrome.

A 7-year-old girl was diagnosed with trichothiodystrophy due to low sulfur levels in her hair.

Monilethrix hair issues are due to problems in the hair's internodes.

Patients with alopecia areata and eosinophilia have more nail issues and severe hair loss.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Prolonged use of topical corticosteroids can cause excessive hair growth.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

An 11-year-old girl with hair thinning was diagnosed with monilethrix and early androgenetic alopecia.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Loose Anagen Hair syndrome occurs in dark-skinned children and often improves on its own.