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Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

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

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Thyroid disease can cause hair loss and treating thyroid problems might help with hair disorders.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Botox increased hair count in men with baldness and might work by improving scalp blood flow.

Oral minoxidil shows promise in treating monilethrix-related hair loss.

Some horses lose hair without inflammation or itching due to various conditions, and while mainly a cosmetic issue, diagnosis requires examination and biopsies, and breeding is not advised if it's hereditary.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Minoxidil and finasteride effectively treat hair loss.

Different women's hair and skin glands respond to hormones in varied ways, which can cause unwanted hair growth even with normal hormone levels, and more research is needed to treat this effectively.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Secukinumab for psoriasis unexpectedly caused increased hair growth in a patient.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

Short anagen syndrome involves a hair growth phase lasting 1.5 years.

Hair loss can indicate or worsen with systemic diseases, and treating the underlying condition is important.

Antigens from skin cells may cause hair loss in perinevoid alopecia.

Lipase H is important for hair follicle function and shaping hair fibers.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

Trichoscopy is a key method for dermatologists to quickly and effectively diagnose hair and scalp conditions.

Lupus panniculitis of the scalp causes linear hair loss and needs ongoing treatment to prevent recurrence and lupus.

Researchers found a gene mutation responsible for a rare hair loss condition.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.