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The guidelines suggest a detailed approach to diagnosing and treating lupus, with a focus on regular check-ups, personalized medicine, and a range of drug options for different cases.

Using CDK inhibitors on rats showed a reduction in chemotherapy-caused hair loss, but later experiments could not repeat these results.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

Notch-related genes play a key role in the development and cycling of hair follicles.

Different types of hairs on a rat's hindlimb have varying levels and patterns of nerve innervation.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

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

Women with severe types of PCOS are more likely to have metabolic syndrome, and belly fat is a key predictor of this risk.

Researchers developed a mouse model that successfully mimics the bladder damage seen in humans after radiation therapy.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

Researchers created a lab model to study human hair growth, showing it can grow and self-regulate outside the body.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

A man had two rare autoimmune diseases that might be connected.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

Sunlight exposure improved a patient's skin condition, and there may be a link between a certain disease and skin growths; a leukemia treatment caused changes in hair color and growth.

Boxer dogs may have a genetic skin condition that worsens seasonally and can be treated with certain medications.

The document concludes that successful management of eyebrow and forehead ptosis requires a thorough approach, considering anatomy, patient evaluation, and careful selection of surgical techniques.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

Human foreskin does not show aging or reduced cell growth after radiation, and H2A.J is not a good marker for radiation-induced aging.

People with Type 2 Diabetes are more likely to have a mite infestation called Demodex folliculorum.

A unique case showed a rare combination of two types of lichen planus on the face.

A three-year-old girl has hair loss despite treatment with selenium sulfide shampoo and anti-fungal medication.

Combining PRS with TAFR is promising for treating complex fistulas, with most patients achieving long-term healing.

A man had a large, rare cyst in his mouth removed after 10 years, which fixed his swallowing and breathing problems.

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

A young Persian cat had a skin infection and low platelets, treated with various medications.

The herbal hair oil may improve hair shine and address hair issues, but its effectiveness is unclear.

A woman's rare benign eyelid tumor was correctly identified through detailed tissue analysis.