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A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

BI 2536 had limited effectiveness against several advanced cancers and caused significant side effects.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Imatinib can cause hair loss due to lichen planopilaris.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A mutation in mice causes hair loss and immune problems.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

TCF7L2 gene polymorphism is linked to alopecia areata, but it doesn't affect the success of PRP or conventional treatments.

Uterine leiomyomas don't significantly change gene expression in the scalp of people with Central Centrifugal Cicatricial Alopecia.

High CCL11 levels may indicate poor response to baricitinib in severe alopecia areata.

CD44 variant changes start alopecia areata, but don't maintain it.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

Vismodegib is effective for basal cell carcinoma but has severe side effects.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

Basal cell carcinomas may differentiate similarly to hair follicles and could be influenced by hair cycle-related treatments.

Certain immune markers may predict chemotherapy response in mesothelioma, and nivolumab is a tolerable and effective treatment for advanced non-small cell lung cancer.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

The genes OVOL1 and OVOL2 are important for hair growth and may be involved in a type of skin tumor.

A man developed oral hairy leukoplakia while on baricitinib, a medication for alopecia and arthritis, and doctors should watch for such side effects.

Bicalutamide may be a promising alternative treatment for female pattern hair loss.

MC4R gene variants not linked to female hair loss.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.