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Recurrent NICF is a rare skin condition with unclear causes, involving follicle inflammation and crystal deposits.

The infant likely has Hay-Wells syndrome and needs genetic testing and heart screening.

Intralesional cidofovir may be a viable alternative treatment for SCC.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Aged Julia Creek dunnarts suffer from reproductive and hormonal issues, aiding conservation efforts.

A new gene variant in a girl with Coffin-Lowry Syndrome may link the condition to early puberty.

Metallothionein likely helps in cell growth and development in wool follicles of fetal sheep.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

A 65-year-old man with sudden abdominal pain and seizures was diagnosed with a rare, non-traumatic splenic rupture and treated without surgery.

An elderly woman with cancer improved after treatment for a rare skin condition with coiled hairs.

The hypothesis suggests that PCOS may start early in life due to genetic and environmental factors, influencing future reproductive and metabolic problems.

Women with PCOS have higher risks of heart disease, type 2 diabetes, and endometrial cancer.

Cervi Parvum Cornu complex improved urinary symptoms in men without major side effects.

Too much male hormone in mothers can negatively affect the sexual behavior of both male and female baby mice.

A child's toe was saved from a rare condition where hair tightly wrapped around it by performing surgery.

Monilethrix hair issues are due to problems in the hair's internodes.

Amenorrhea, or the absence of periods, should be evaluated by age 15 or within five years of early breast development, and is most commonly caused by conditions like polycystic ovary syndrome and hypothalamic amenorrhea.

A simple screening method found that 6.3% of women in a semiurban area in Sri Lanka have polycystic ovary syndrome, with most showing menstrual irregularities.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

Menstrual disorders are common in adolescents and can be influenced by weight, activity, and health issues, requiring careful evaluation and more research for effective treatment.

PCOS requires personalized treatment to improve life quality and reduce health risks.

Matriptase is highly active in hair follicles and sebaceous glands, especially during hair growth phases.

Ovarian vein sampling helped diagnose rare ovarian tumors causing high testosterone, and surgery to remove the tumors lowered the testosterone levels.

A young cat had a rare hair condition with twisted hair shafts but stayed healthy.

The new rodent model successfully mimics non-lean human PCOS symptoms.

Congenital triangular alopecia is a harmless, non-spreading hair loss condition often seen in young children.

Hair shaft changes may be linked to CCCA, but their role is unclear.