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A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

Woman's hair loss diagnosis changed from CTE to AA; multiple biopsies important for accurate diagnosis.

Dermoscopy helps diagnose syphilitic alopecia, and treatment with penicillin can regrow hair.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

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

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

PCOS is a long-term condition that needs more research for better understanding and treatment.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

A gluten-free diet stopped a child's hair-eating behavior and suggested she had celiac disease.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

Doctors don't use trichoscopy enough, even though it's good for diagnosing hair problems.

A 3-year-old boy lost all his hair due to a rare reaction to phenobarbital, but it grew back after steroid treatment.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Diagnosing and managing PCOS in teens is hard, but early diagnosis and lifestyle changes are key, and more research is needed for long-term health.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

Fluridil promotes hair growth safely and effectively for androgenetic alopecia.

Eating more protein during fast weight loss can prevent hair loss.

The study suggests that complement activation, not immunoglobulins, may be important in erythema nodosum leprosum.

An 8-year-old boy recovered from a rare case of penile tourniquet syndrome after hair removal surgery.

Serenoa repens may cause early puberty and should be used cautiously in children.

Pre-operative hormone treatment for hypospadias surgery might improve outcomes, but more research is needed to confirm.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

The document recommends a team-based approach and personalized care for managing diabetes in teenagers.

Spironolactone may help treat excessive hair growth in girls, but more research is needed.

Biotin helps regulate proteins in the blood, which may explain its role in hair growth.

Malnutrition can cause unusual eyelash growth and hair loss.

Green tea extract may help reduce excessive hair growth.