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Merkel cells and Langerhans cells in hair follicles are closely connected and may interact.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Accurate diagnosis is key for treating different kinds of hair loss, and immune response variations may affect the condition and treatment results.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

Hair follicle development is controlled by interactions between skin tissues and specific molecular signals.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

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

Alopecia areata is a type of hair loss that can lead to complete baldness, often associated with other autoimmune conditions, and half of the cases may see hair return within a year.

Scientists created stem cells that can grow hair and skin.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Scarring alopecias are complex hair loss disorders that require early treatment to prevent permanent hair loss.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Acitretin helped improve hand mobility and skin condition in a patient.

Androgens contribute to common male hair loss; more research needed for hair growth medication.

The study found that pili bifurcati causes hair to intermittently split into two branches, each with its own outer layer.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

The document explains the genetic causes and characteristics of inherited hair disorders.

Understanding fetal skin development helps diagnose congenital skin diseases.

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.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The document is a detailed medical reference on skin and genetic disorders.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.