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The patient with severe hirsutism improved after being diagnosed with non-classic congenital adrenal hyperplasia and treated with corticosteroids.

A patient with congenital adrenal hyperplasia improved after adjusting her medication to prevent Cushing's syndrome symptoms.

A hair growth ointment improved hair length in a family with a genetic hair growth condition.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Björnstad syndrome causes twisted hair from birth.

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.

Some scalp sores are linked to different inherited skin conditions.

Alopecia in animals can be hereditary, congenital, or acquired, with treatments and outcomes varying widely.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

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

Untreated congenital adrenal hyperplasia can lead to complications like stroke and needs glucocorticoid treatment.

Understanding fetal skin development helps diagnose congenital skin diseases.

The document concludes that doctors should recognize congenital triangular alopecia to avoid unnecessary treatments, as it does not respond to steroids like alopecia areata does.

Polycystic Ovary Syndrome (PCOS) is common in women with conditions like anovulation, hirsutism, hair loss, and type 2 diabetes, and it can lead to health risks like heart disease, obesity, insulin resistance, and depression. Non-Classic Congenital Adrenal Hyperplasia (NC-CAH) is also discussed.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

HDPCM treatment healed a baby's congenital skin defect caused by varicella infection.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Minoxidil is better for female hair loss without hormonal issues, cyproterone acetate for those with; people with treated congenital heart disease have lower life quality; personality differs in types of infertility; oral terbinafine is best for toenail fungus; bladder training reduces incontinence; nurse clinics help with heart disease; weight loss improves body composition and liver disease; computer training cuts drug errors.

Cantú syndrome is caused by mutations in the ABCC9 gene.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

The document explains the types of excessive hair growth and how to manage it.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.