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An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

The authors maintain there is a significant link between vitamin D deficiency and central centrifugal cicatricial alopecia in Black patients, and call for more research on the topic.

Different γδ T cell types have unique roles in causing alopecia areata.

Oral zinc therapy is effective for treating acrodermatitis enteropathica.

A20 protein is crucial for normal skin and hair development.

CD90 is present on specific cells in dog hair follicles.

Two sisters had a rare hair condition without other usual symptoms.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

Prednisolone and Bactrim improved symptoms in a woman with Cronkhite-Canada syndrome.

A woman with discoid lupus improved with treatment after being misdiagnosed with a different hair loss condition.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

Vitamin A supplements improved skin and health issues in dogs.

People with HIV and low T cell counts have more hair and scalp problems.

Early diagnosis and a strict gluten-free diet are crucial for children with celiac disease to improve symptoms.

The meeting covered new findings in children's skin conditions and treatments, including the benefits of super absorbent polymer diapers.

The LMNA mutation affects skin structure even in asymptomatic carriers.

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

DGAT1 enzyme is crucial for healthy skin and hair by regulating retinoid levels.

Malondialdehyde-modified DNA may trigger an immune response in alopecia areata patients.

An 84-year-old man developed severe anemia after his first COVID-19 vaccine shot, improved with treatment, and was advised against a second dose.

Vitamin B12 deficiency can cause reversible hair color loss in children.

Cronkhite-Canada Syndrome often leads to death within 6-18 months.

People living with HIV in Turkey often have skin conditions, which are more common in advanced HIV stages and may help in diagnosing the infection.

Antifungal treatment can improve severe skin infections with cutaneous horns.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

CD4+ lymphocytopenia can occur in patients with systemic lupus erythematosus.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.