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No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.

Celiac disease can cause skin problems that may get better with a gluten-free diet.

FOXN1 gene variants cause low T cells and immune issues from birth.

A 10-year-old girl with Fox Fordyce disease improved with treatment, suggesting the disease can occur before puberty and might be underdiagnosed in young girls.

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

UVA1-light therapy successfully treated a child's skin condition, mycosis fungoides.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

Fox Fordyce disease can occur in prepubertal girls and may be underdiagnosed.

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

The document concludes that identifying the cause of eyebrow and eyelash loss is key to treating it and improving quality of life.

Hair follicles are complex, dynamic mini-organs that help us understand cell growth, death, migration, and differentiation, as well as tissue regeneration and tumor biology.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

The HR protein's role as a repressor is essential for controlling hair growth.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Hormone imbalances can cause specific skin changes, which may help in early detection of endocrine disorders.

Thyroid hormone affects skin health, with too little causing rough, pale skin and too much leading to smooth, thin skin, and may also impact wound healing and skin conditions.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

RT1640 treatment reverses gray hair and promotes hair growth in mice.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Iron deficiency might contribute to hair loss in women.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The document explains various skin conditions and their treatments.

Itch is a common symptom in patients with chronic venous insufficiency, often accompanied by burning and pain.

Itch is a common symptom in patients with chronic venous insufficiency, often worsening with standing or sitting and occurring mostly in the evening or at night.

Mycophenolate mofetil improved skin condition in a man with nephrogenic fibrosing dermopathy.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Botulinum toxin type A significantly reduces scalp psoriasis severity compared to placebo.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.