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Mycosis fungoides can have unusual symptoms and may be misdiagnosed, but specific cell markers might suggest a lower risk of worsening.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

Kindler Syndrome shows diverse symptoms and needs better diagnostic tools and care in resource-limited areas.

T cells affect skin cell genes in inflammatory diseases, and therapy can normalize these changes.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

The research found a new way to heal chronic skin ulcers by turning certain cells into skin tissue using specific factors.

Lack of certain fatty acids causes skin, immune, and fertility issues in mice.

In 2017, pediatric dermatology advanced with new treatments and insights into various skin conditions in children.

A man had two rare autoimmune diseases that might be connected.

The protein interleukin-1 alpha helps regenerate hair follicles and increase stem cell growth in mice.

ILC1-like cells can cause alopecia areata by disrupting hair follicle immunity, suggesting a new treatment approach.

SLE in ageing patients is less severe and needs careful treatment to avoid excess.

Dkk genes evolved faster in birds and reptiles, affecting hair development functions.

An adult with a rare skin condition improved with tazarotene treatment.

Mitochondrial dysfunction is linked to various skin conditions and could be a target for treatments.

A woman with myotonic dystrophy had multiple skin tumors on her scalp, suggesting a genetic link.

A new mouse mutation causes skin and hair defects due to a gene change.

Children with frequent severe infections and low antibodies should be checked for immune deficiencies.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.

Mutations in keratin genes cause skin, hair, and nail disorders, with future treatments possible.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

A girl with symptoms like an autoimmune disorder actually had HIV and a fungal infection, which was hard to diagnose and treat, leading to her death.

Chromosomal changes, including those in the WRN gene and rDNA, may significantly contribute to aging.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

Permanent hair loss after bone marrow transplant can be caused by chemotherapy or chronic graft-versus-host disease.

A man with a rare disease experienced late hair whitening and loss, but hair color returned, suggesting a good outlook.

Nerve fibers may worsen mast cell activity, leading to abnormal elastic fiber buildup from sun exposure.