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Early diagnosis and lifelong zinc supplementation are crucial for treating acrodermatitis enteropathica effectively.

Narrowband UVB therapy significantly improved a child's rare skin condition.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

A gene mutation in Lama3 is linked to a common type of hair loss.

More research is needed to understand how testosterone is maintained in adult males.

Certain surgical methods are better than routine incision for hidradenitis suppurativa, topical clindamycin and acitretin are effective treatments, men with HS have a risk of skin cancer, HS patients are more likely to die from heart problems, and specific genetic markers are linked to treatment response.

The document concludes that managing Dunnigan-Type Familial Partial Lipodystrophy involves treating associated health issues and using medications like metformin and leptin replacement.

Mutations in the AR gene cause hair thinning and loss.

Modulating Cytochrome P450 activity could help develop new skin disease treatments.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

A patient with a scalp condition and benign skin tumor experienced hair loss and did not improve with treatment, choosing not to have surgery despite a small cancer risk.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Olfactory receptors found outside the nose may offer new treatments for diseases like cancer and help in wound healing and hair growth.

Hair growth and development are controlled by specific signaling pathways.

Alopecia areata is caused by immune system attacks on hair follicles, often triggered by viral infections.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

A new 3D culture system helps grow and study mouse skin stem cells for a long time.

Women may need different blood pressure guidelines than men for heart disease prevention.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.