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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Keratin proteins in epithelial cells are dynamic and crucial for cell processes and disease understanding.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

New treatments targeting specific genes show promise for treating keratin disorders.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

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

Skin problems can be caused or worsened by physical forces and pressure on the skin.

Isotretinoin may effectively treat hereditary hypotrichosis simplex, a rare hair loss condition.

Mutations in keratin genes cause cell fragility and various skin disorders.

Keratin mutations cause skin diseases and could lead to new treatments.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

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

Epidermolysis bullosa is a genetic disease causing fragile skin and blisters in both animals and humans.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

Combining PRP injections with minoxidil 2% effectively promotes hair growth in hereditary hair loss.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

The document's conclusion cannot be provided because the document is not available or cannot be understood.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

A woman lost her hair after taking acyclovir, but it grew back when she stopped the medication.

Dandruff might be caused by changes in how hair follicles naturally release oils and an immune response to this imbalance.

Zinc pyrithione needs targeted delivery to the scalp for effective dandruff treatment.

Reflectance confocal microscopy can tell apart white dots on the scalp as either sweat gland ducts or hair follicle openings.

Skin problems are common in Bangladesh due to arsenic, prompt treatment of diabetic foot ulcers is crucial, maternal transmission causes most neonatal herpes, treatments for pediatric vasculitis are effective, the chickenpox vaccine works, more frequent UVB therapy helps psoriasis, certain jobs increase hand dermatitis risk, monoclonal antibodies treat psoriasis well, lifestyle affects psoriasis, alefacept improves psoriasis, imiquimod cream partially clears basal cell carcinoma, and iron may not help chronic hair loss.

Spironolactone is effective for treating acne, hirsutism, and androgenic alopecia in women with few side effects.