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A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

Different types of female pattern hair loss have unique characteristics and are associated with various health conditions.

Low-dose oral minoxidil may help children with short anagen syndrome grow longer hair.

People with androgenetic alopecia have an imbalance in their autonomic nervous system activity.

A 46-year-old man was diagnosed with frontal fibrosing alopecia, a condition usually seen in postmenopausal women.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

A kidney transplant patient developed leprosy, likely due to immunosuppression and genetic factors, and improved with treatment.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Different connective tissue disorders have unique symptoms and treatments, with varying outcomes and often require ongoing care from a specialist.

Trichoscopy helps distinguish Lichen Planopilaris from Frontal Fibrosing Alopecia by identifying unique hair loss patterns.

New hair loss subtype found, mimics common baldness.

Syphilis can mimic other diseases, making diagnosis challenging, but proper testing and treatment are effective.

A rare form of lupus caused hair loss and skin bumps, diagnosed through biopsy, improved partially with treatment.

PUVA treatment may have triggered lupus in a woman with psoriasis.

Progeria, a disease that causes early aging, is linked to a gene mutation and helps us understand normal aging.

Early detection and aggressive treatment of severe lung complications in lupus are crucial to improve survival.

Certain RNAs may help diagnose alopecia areata by affecting keratin genes.

A machine learning model can predict scarring in lichen planopilaris using factors like vitamin D levels and diagnostic delay.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

A young woman with lupus developed tuberculosis due to weakened immunity from her medication, showing the need for better TB screening in such patients.

A woman's severe male hormone excess was caused by a small, hard-to-find ovarian tumor.

Mitochondrial dysfunction may contribute to chronic inflammation and immune system issues in Lichen planopilaris.

The study found a link between the severity of Lichen Planopilaris seen by doctors and the details seen under a microscope, and created a new way to measure this severity.

Japanese cases of fibrosing alopecia show a unique age and hair loss pattern, possibly due to racial differences.

The study found that Short Anagen Syndrome results in short hair growth not due to hair fragility, and hair may grow longer after puberty.

Shiny white structures in trichoscopy can indicate long-standing discoid lupus erythematosus alopecia.

A teenage girl had both a rare ovarian tumor and a severe form of polycystic ovarian syndrome.

Defective nuclear transport may cause gene expression changes in Progeria.

Basement membrane changes in lichen planopilaris cause scarring and permanent hair loss.