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Dihydrotestosterone and 5α-Reductase play a role in hair loss and prostate health, and finasteride can increase hair growth in men without affecting sperm production, but it doesn't work for postmenopausal women with hair loss.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

The document concludes that early and accurate diagnosis of hair loss on the top of the scalp in Black men is important to distinguish CCCA from other types of hair loss.

The study suggests that analyzing DNA can help treat hair loss, but more research is needed.

Hair graying may be caused by stem cell depletion from stress or melanocyte damage.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

Minoxidil, originally a blood pressure medication, is effective in treating hair loss in men and women, with different strengths recommended for each.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Dupilumab helped improve skin and prevent new lesions in a child with a rare immune disorder and severe eczema.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

Skin problems are common in Lupus patients and can indicate the disease's severity, requiring specific treatments and lifestyle changes.

The document concludes that understanding the sebaceous gland's development and function is key to addressing related skin diseases and aging effects.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Trichoscopy helps tell apart Frontal Fibrosing Alopecia and Lichen planopilaris by showing different hair and scalp features.

Exosome treatment safely increases hair density in male patients with androgenetic alopecia.

Collagen is crucial for health and treating certain diseases, and supplements can improve skin, nails, and hair conditions.

A woman with lupus had muscle weakness due to kidney issues and was successfully treated with medication.

Dermoscopy helps accurately diagnose temporal triangular alopecia, avoiding unnecessary treatments.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Thyroid disease can cause skin, hair, and nail problems, and treating the thyroid condition often improves these symptoms.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.