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Pili annulati is caused by a protein metabolism disorder affecting hair structure.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

New therapies and trials are needed for Merkel cell carcinoma, a tough skin cancer.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Mouse skin has special cells in the epidermis that decrease with age and are linked to keratinocyte stem cells.

Trichodysplasia spinulosa can occur after a heart transplant due to immunosuppressive drugs.

Mutations in Far2 mice cause hair loss due to sebaceous gland issues.

Malassezia-associated dermatitis can cause itching in cats with feline paraneoplastic alopecia.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Skin conditions in multiple myeloma patients vary with the timing of bone marrow transplants.

An elderly man with skin amyloidosis and abnormal blood proteins was monitored without finding widespread disease after 18 months.

Even a small melanoma can be deadly if not removed, regardless of the patient's age.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

A man had a rare skin cancer that looked like a bald spot.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

Accurate diagnosis of rare scalp cancer requires combining clinical and radiological information.

Congenital triangular alopecia is a harmless, non-spreading hair loss condition often seen in young children.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

A 60-year-old man with Cronkhite-Canada syndrome improved with treatment, but the condition has a high mortality rate and a risk of colorectal cancer.

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

A woman got melanoma on her scalp after anti-hair loss treatment with injections.

A rare skin cancer on a man's elbow was successfully treated with surgery, showing no recurrence after one year.

Hair follicles can be used to easily create neurons and glial cells for potential nerve repair.

Trichoscopy is a helpful tool for diagnosing Netherton syndrome.

Two Hispanic women developed Plica neuropathica, a condition causing tangled hair, possibly due to hair damage and various risk factors.

Men with certain types of baldness at age 45 may have a higher risk of colon cancer and colorectal adenoma.

Human hair keratin hydrogel may aid nerve repair better than traditional methods.

A man had four testicles, two of which were outside the scrotum and looked like fatty lumps.