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Stem cells improve healing of diabetic wounds.

Neck burn scar contracture recurrence is more likely with larger neck defects, and closer follow-up can help detect it sooner.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Pre-surgical embolization and a two-stage resection improve outcomes for rare sacral tumors.

Adequate steroid treatment needed to limit bone loss in PMR patients.

Bicalutamide is more effective and safer than spironolactone for treating female hair loss.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

An elderly woman's swollen, painful foot was found to be caused by a rare type of bone lymphoma, which improved with radiation treatment.

Children with alopecia areata have lower BDNF levels, linked to worse symptoms and quality of life.

The PEEK cage reduced pain more than the dynamic cervical implant, but the implant allowed slightly better movement after surgery.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

Home photobiomodulation therapy can improve life quality and mobility for disabled individuals.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

Bicalutamide mesotherapy improved hair density in women with hair loss and was well received.

PBM helps improve cell survival in 3D tissue engineering.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

BAP1 mutations are rare in pediatric melanocytic tumors and may develop later in life.

Hypothyroidism may cause vertigo symptoms like BPPV.

PBM therapy improves mitochondrial function and promotes tissue regeneration in dental pulp stem cells.

Bone marrow and hair follicle cells help form skin tumors, suggesting new treatment targets.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

Björnstad syndrome can cause hair loss similar to androgenetic alopecia, and treatment with baricitinib and minoxidil may help.

BMP2 needs periosteal tissue to help regenerate mouse middle finger bones within a specific time.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

High-intensity red LED light boosts bone cell growth and mineralization.

Bortezomib chemotherapy can cause temporary skin rashes.