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Alopecia areata is an autoimmune disease where T cells attack hair follicles.

The document concludes that alopecia areata is an autoimmune disease without a definitive cure, but treatments like corticosteroids are commonly used.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

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.

Early diagnosis and treatment, using finasteride, minoxidil, or hair transplantation, improves hair loss outcomes.

Effective hair loss treatment in women requires correct diagnosis and can include medications like minoxidil, antiandrogens, and treatments for underlying conditions like PCOS.

Alopecia common in teens, may indicate endocrine issue, minoxidil effective treatment.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

Heredity and hormones cause common hair loss, and topical minoxidil is the first recommended treatment.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

The document concludes that managing skin conditions during pregnancy is important and requires specialized care.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

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

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

Early intervention and patient education are crucial for managing alopecia areata.

Hashimoto thyroiditis is an autoimmune disease that can lead to an underactive thyroid and is treated with medication and sometimes diet changes or surgery.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Alopecia areata is a common autoimmune disease affecting about 2% of people, causing significant disability and often associated with mental health issues and other autoimmune conditions.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

Alopecia Areata is an autoimmune condition causing hair loss, influenced by genetics, environment, and possibly improved by anti-MIF therapy, with many patients experiencing regrowth within a year.

CO2 laser treatment for aging skin significantly changes immune system-related genes.

A protein called lfTSLP is important in causing allergic and other skin diseases and could be a target for treatment.

Finasteride may cause lasting sexual and mental health issues, and genetic screening could help prevent them.