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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 new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Trichoscopy effectively diagnoses and assesses the severity of androgenetic alopecia.

Hair loss affects women's self-esteem; treatments like minoxidil can help.

The document discusses male and female pattern hair loss, its diagnosis methods, FDA-approved treatments like finasteride and minoxidil, their side effects, and the role of lifestyle changes.

Cancer patients treated with immune checkpoint inhibitors may develop alopecia, but some hair regrowth is possible with treatment.

Hair transplants are highly satisfactory for treating female-pattern hair loss.

The conclusion is that dermatologists can improve women's skin health but must overcome cultural and economic barriers to do so.

Topical minoxidil helped an 8-year-old boy with a genetic hair disorder grow hair.

Hedgehog pathway inhibitors used for skin cancer can cause significant hair loss, which may improve after stopping the medication.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Minoxidil and finasteride effectively treat hair loss.

Hormone therapy affects hair growth in transgender individuals, with testosterone potentially causing hair loss in trans men and estrogen reducing facial/body hair in trans women; treatment options vary.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Alopecia areata causes unpredictable hair loss and emotional distress, with no cure and limited treatment options.

Recent progress has been made in understanding inherited hair and nail disorders.

Alopecia is linked to various health and mental conditions, impacts life quality, and needs medical attention beyond its cosmetic effects.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Online skin care companies offer easy access to treatments but may have ethical issues like confirming patient identity, prescribing unproven therapies, and not fully explaining medication side effects. They should prioritize patient care over profit.

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

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Hair transplantation is an effective hair loss treatment with two main techniques, requires careful planning, and can improve beard and eyebrows appearance.

A 9-month-old baby had a rare, persistent ring-shaped hair loss condition.

Addressing concerns about side effects, cost, and long-term use could improve minoxidil treatment adherence.

Monilethrix is a rare genetic hair disorder that's hard to treat.

Mitochondrial dysfunction links metabolic syndrome and inflammatory skin diseases, suggesting targeted therapies and lifestyle changes.

The 810-nm diode laser improves skin texture in keratosis pilaris but not redness.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.