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Mogamulizumab can cause hair loss and skin rashes.

Excessive minoxidil use can damage hair structure.

Congenital triangular alopecia and vitiligo can occur together, but treatment for one may not affect the other.

Early diagnosis using eye tests and lab markers can improve treatment for pediatric Sjögren's syndrome.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.

Minoxidil can cause temporary vision loss and color blindness.

Molluscum contagiosum can occur in epidermoid cysts, especially with prolonged steroid use.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

Selumetinib significantly reduced tumor size and improved vision in a child with neurofibromatosis type 1.

MCHR2 gene duplications may be linked to alopecia areata.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

Hair transplant surgery successfully restored a boy's moustache hair on a cleft lip scar, with natural-looking results and patient satisfaction.

Drug misuse can cause serious eye infections and other severe side effects.

Sudden, unusual hair loss may indicate serious underlying health issues.

Cystic panfolliculoma is a rare, harmless tumor that can be confused with other skin tumors.

Removing certain muscles during a browlift reduces glabellar wrinkles better long-term.

Reticular erythematous mucinosis syndrome can occur with minimal mucin deposition.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Temporal triangular alopecia usually starts in early childhood and treatment with Minoxidil has limited effectiveness.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

Eyelash loss can be a sign of thyroid problems.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

Hair transplant surgery successfully restored a boy's moustache hair on a cleft lip scar, with natural-looking results and patient satisfaction.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

The patient with EEC syndrome had scarring alopecia due to deep folliculitis, possibly linked to abnormal hair structure.

Bilateral ovarian hyperthecosis is a rare but treatable cause of increased facial hair in postmenopausal women.