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Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Self-amplifying RNA could be a better option for protein replacement therapy with lower doses and lasting effects, but delivering it into cells is still challenging.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

Pattern hair loss is mainly caused by genetics and hormones, with limited effective treatments available.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

The study concluded that key signs of Keratosis follicularis spinulosa decalvans are changes in terminal hair and vellus hair follicles, which likely start the inflammation and damage to hair follicles.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

Some people with alopecia areata, a hair loss condition, get better within a year without treatment, but it can happen again.

Female pattern hair loss is common, often starts in the 30s or 40s, worsens after menopause, and can negatively affect quality of life.

Hirsutism is often caused by high male hormone levels and can be treated with lifestyle changes and medications.

A new food supplement was highly effective in curing hair loss in young men.

The emulgel with specific ingredients was effective for treating hair loss.

Loose Anagen Syndrome causes easy-to-pull, thin hair, mainly in young girls, and improves with age.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Cats can get skin issues from things other than fleas, like insect bites, food, or allergens.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

The article concluded that choosing the right surgical method based on a patient's specific needs can make the lower eyelid look younger.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

Cytochrome P-450 enzymes in the skin help break down various substances and could be targeted to treat skin conditions.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Both genetics and lifestyle factors contribute to male pattern baldness.

Early recognition and management of connective tissue diseases like lupus are crucial in young patients.

A 14-year-old boy is the youngest person reported with a rare, benign tumor related to hair follicles, usually found in older people.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

Light therapy may improve eye conditions by stimulating cell activity and increasing oxygen availability.

A Thai Bangkaew dog with diabetes and pancreatic issues improved with insulin, enzymes, and vitamins.