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Intralesional corticosteroids and 5-alpha-reductase inhibitors are the best treatments for frontal fibrosing alopecia.

Caffeine may help hair growth in hereditary hair loss.

Dermatology residents need better training to treat hair conditions in patients with skin of color.

Synthetic hair implants can cause infection and scarring, so safer options like follicular unit excision are recommended.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Androgenic alopecia causes hair thinning, and treatments include minoxidil, finasteride, and light therapy.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Testosterone undecanoate safely and effectively increased penis size in male children with 5-alpha-reductase deficiency.

The procedure effectively created natural-looking hairlines and improved facial balance in female patients.

A pregnant woman with Werner's syndrome died during childbirth, but her baby survived and did not have the syndrome.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Oral retinoic acid effectively treated collodion baby, with hair loss as the main side effect.

Frontal fibrosing alopecia is a challenging hair loss condition with no known cause or definitive treatment.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Monitoring potassium levels is important for women taking spironolactone.

Autoimmune polyglandular syndrome can cause temporary brain issues that may improve on their own.

The study found different balding patterns in men of color.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Skin diseases look different on pigmented and nonpigmented skin.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Dermatologists should monitor potassium levels in women taking spironolactone for acne, hair loss, and hirsutism.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

Dermoscopy helps diagnose frontal fibrosing alopecia by distinguishing it from other hair loss conditions.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Intralesional triamcinolone injections can effectively stop frontal fibrosing alopecia with minimal side effects.

Treatments for hair loss vary, but cell-based options may be the future.