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MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Differences in gene expression and methylation patterns found in AGA patients suggest potential targets for future treatments.

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.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Skin problems are common in Lupus patients and can indicate the disease's severity, requiring specific treatments and lifestyle changes.

Ovulation disorders are a major cause of infertility and menstrual problems in women.

Stopping forehead irritation and using hydrocortisone helped a man's skin, Martinique has lower melanoma rates, a man had an allergy to a specific antifungal, another had unexplained cysts, certain drugs can cause skin reactions without always being interrelated, a link between Fanconi anemia and a skin condition was suggested, high levels of a certain protein may play a role in a type of psoriasis, and there's a need to study the connection between scalp pain and hair loss.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Tiny RNA molecules help control the growth of plant hairs.

Adequate vitamin D might lower, and high hair chromium might increase DNA damage in obese women.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

Babies were mostly born healthy from fathers who took finasteride, but some pregnancies ended early; more research is needed.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Male androgenetic alopecia involves hair follicle miniaturization due to DHT, with potential treatments using inhibitors and blockers.

Dermatopathology has made significant progress but many skin diseases remain incurable, requiring ongoing research.

Animal research has greatly advanced dermatology.

A 3-month treatment improved PCOS symptoms and reduced certain immune proteins.

MSC-protein helps regenerate gum tissue and bone.

More research is needed to understand sex and racial differences in long COVID.

A new gene mutation causes insulin resistance in a girl and her mother.

Robotic hair transplantation with AI offers more reliable, precise, and efficient hair restoration.

A new gene variant causes glucocorticoid resistance in a mother and son.

People with Down syndrome have higher rates of certain immune-related conditions and need special medical attention.

The safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

Long-COVID has diverse, long-term health impacts, especially in young people.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.