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The document concludes that hair loss in cats is caused by various factors, including allergies, mites, infections, and hormonal issues, with treatments varying accordingly.

Some drugs can cause changes to your hair.

Early baldness in men may indicate risks for obesity, metabolic syndrome, insulin resistance, and heart disease, similar to women with PCOS. Alopecia areata is often linked with autoimmune diseases and mental health issues. Certain hair disorders are due to genetic issues, and chemotherapy can cause hair loss through specific biological pathways. Iron deficiency's link to hair loss is still disputed.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

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.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Benzoyl peroxide and adapalene gels work differently to reduce acne in mice.

Hair follicle stem cells in hairpoor mice are disrupted, causing hair loss.

The article suggests that hair transplant surgery may not be purely cosmetic because it treats a disease and calls for clearer guidelines on its classification.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

The document is a detailed guide on skin conditions and treatments for dermatologists.

Trichoepitheliomas can be hard to distinguish from other skin conditions and often start in teenage years.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Three dogs with a rare skin condition improved with treatment.

The document concludes that understanding and managing hair loss in cancer patients is important, and more research is needed for better treatments.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Malnutrition can cause unusual eyelash growth and hair loss.

Researchers identified specific genes that are important for mouse skin cell development and healing.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

The study concluded that similar pathways regulate hair growth in dogs and mice, and these pathways are disrupted in dogs with Alopecia X, affecting stem cells and hormone metabolism.

A girl with Netherton syndrome was able to eat wheat without allergies after a special treatment.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

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