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There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

A woman lost over 80% of her hair due to a condition called telogen effluvium after having COVID-19.

A woman's male-like physical changes were caused by two rare ovarian conditions.

People with Down syndrome have a higher risk of skin disorders and need better screening and treatment.

A man with four autoimmune diseases suggests a new category for multiple autoimmune syndrome.

EPDS is a rare, chronic scalp condition that's hard to treat and needs better awareness for improved outcomes.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

Patients with one autoimmune disease should be checked for other autoimmune disorders.

The study concluded that a new method can effectively assess scalp sun damage in balding men, which increases with age and sun exposure.

The document says that early treatment of Acne Vulgaris is important to prevent scarring and that adult onset acne is common in women, often due to hormonal imbalances.

The document concludes that proper recognition and treatment of skin appendage disorders are important for management.

Eating disorders are serious, often undiagnosed conditions requiring early treatment, with anorexia being the most deadly and binge-eating the most treatable.

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

Ovarian steroid cell tumors should be considered in adults with hirsutism and high testosterone, with surgery as the main treatment.

Skin symptoms can indicate endocrine disorders and have various treatments.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

The conclusion suggests that the zinc lozenge study is valid despite imperfect blinding, as many participants could not correctly identify their lozenge type.

The document concludes that more research is needed on the hepatitis B vaccine's side effects and the effectiveness of certain treatments for specific diseases.

Detailed history and physical examination are crucial for diagnosing hair loss.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Patients with Type 1 diabetes should be screened for pernicious anemia.

The document concludes that while white skin, nail, and mucosa diseases increase skin cancer risk, they are generally harmless, especially compared to darker pigmentation conditions.

DM and AA may share a common cause.

Primary cicatricial alopecia, a rare disorder causing permanent hair loss, is hard to diagnose and treat, with treatments like anti-inflammatory drugs and steroids offering varied results and no guaranteed cure. Psychological support for patients is important, and future research should aim to identify causes of the condition.

Deoxycholic acid is FDA-approved for reducing submental fat, but its mechanisms are not fully understood.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

A woman's severe male hormone excess was caused by a small, hard-to-find ovarian tumor.

The conclusion is that having both Frontal Fibrosing Alopecia and Discoid Lupus Erythematosus may suggest a shared immune response in certain people, and a mix of antimalarial drugs and 5-alfa-reductase inhibitors is recommended for treatment.

The document reports the first case of a rare skin condition in Colombia, the 19th case worldwide.

Treating H. pylori infection might help cure alopecia areata.