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An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

The piRNA pathway genes are crucial in early development and may influence sex differentiation through hormone regulation.

A 5-year-old boy's skin condition improved with systemic valganciclovir after a cardiac transplant and immunosuppressive therapy.

The gene causing hair loss and heart issues in rough coat mice is still unknown.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

A 16-year-old boy's alopecia areata progressed unusually to resemble male pattern baldness.

The document reports the first case of a rare skin condition in Colombia, the 19th case worldwide.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Follicular red dots can appear where alopecia areata and vitiligo overlap.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

Erosive lichen sclerosus is a distinct subtype with specific skin features, and treatment led to complete resolution in half of the cases.

Folliculitis Decalvans and Frontal Fibrosing Alopecia can coexist in people with darker skin, showing features of both conditions.

A 7-year-old girl was diagnosed with Netherton's Syndrome, shown by skin and hair symptoms.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

A woman with both TLE and SLE improved with hydroxychloroquine treatment.

Fish teeth and taste bud densities are linked and can change between types due to shared genetic and molecular factors.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Early detection and treatment are crucial to prevent irreversible hair loss in Lichen Planopilaris.

Buffalo flies and Stephanofilaria nematodes cause severe skin lesions in beef cattle, and treatment should target both.

A patient with patchy hair loss was successfully treated for Tumid Lupus Erythematosus after other treatments failed.

LC-OCT helps accurately diagnose different types of infant hair loss without invasive methods.

TAF can be identified by excessive skin thickening and clogged hair follicles, helping distinguish it from similar skin conditions.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.