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Vogt-Koyanagi-Harada disease affects vision and skin, mainly in people with darker skin, and is treated with steroids and immunosuppressants.

Different conditions affect how hair proteins assemble, and certain mutations can change their structure.

Non-itchy rashes can indicate serious diseases like lupus.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

QLT0267 stops hair follicle cell growth and movement.

MC4R gene variants not linked to female hair loss.

The muscle damage was caused by T-cell large granular lymphocytic leukemia, not dermatomyositis.

An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

Melatonin may help with nerve pain, a hepatitis C drug is effective but has side effects, a treatment for mouth sores works but can cause blood issues, ear reconstruction with an implant is safe, HIV transmission from mother to child in Taiwan is now 0% with treatment, certain blood problems are more common in people with a tongue condition, a gene and being overweight are linked to hair loss in some women, a new technique could reduce radiation for lung nodule patients, a hepatitis treatment may lower cancer recurrence after a procedure, and adding extra screening improves tuberculosis detection in patients with lung infections.

Careful monitoring is crucial to prevent JC virus reactivation in lupus patients treated with rituximab.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Machine learning identified three unique subtypes of androgen excess in women with PCOS, each with different metabolic risks.

A 2-year-old girl had a hair disorder not shared by her identical twin.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

The substances improved hair regrowth and protected hair cells in humans and mice.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Lulican™ shampoo is more effective and better tolerated than Ketoconazole for treating scalp seborrheic dermatitis.

The treatment significantly improved lymphocytic cicatricial alopecia symptoms in most patients.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Allergic reactions to blood thinners are rare but can be serious, requiring careful management and alternative treatments.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

Specific immune cells and pathways contribute to hair follicle inflammation and hair loss, suggesting potential treatments for lichen planopilaris.

Scientists found new and known long non-coding RNAs in mouse hair follicle stem cells that may be important for stem cell function and could be targets for cancer treatment.

Being overweight, having gallbladder removal surgery, and taking cholesterol-lowering drugs are linked to a higher chance of getting vulvar lichen sclerosus.

Dermoscopy can non-invasively detect eruptive vellus hair cysts on the labia majora.