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A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

A 17-year-old developed woolly hair nevus in adolescence, which is unusual, and over time the hair darkened and straightened slightly, but microscopic changes persisted.

A rare hair follicle tumor was found on a woman's vulva.

Seborrheic keratoses may partly come from hair follicle cells.

Oncogenic melanocyte stem cells can develop into melanoma similar to human cases.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

Dermoscopy helps diagnose unusual skin lesions like osteonevus of Nanta and can prevent misdiagnosis of serious conditions.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Merkel cell polyomavirus can infect and persist in skin cells, evading the immune system, but certain treatments can control it.

A woman with a long-term skin condition developed a serious skin cancer that led to her death.

Basaloid follicular hamartoma is a rare, benign skin growth often misdiagnosed.

A young woman had a rare scalp tumor usually found in older women.

A rare scalp tumor was removed from a 49-year-old woman, with a good outlook if benign but needing careful monitoring if malignant.

The patient's hair has unique structural differences with alternating bright and dark bands.

A rare type of skin cancer on the scalp can be mistaken for hair loss, causing delayed diagnosis and severe damage.

A boy had a rare scalp condition with thickened skin and different-colored hair.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

A woman with a rare form of multiple myeloma had a headache and a skull mass, which led to her diagnosis after tests and a biopsy.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

The dog's skin condition improved after removing a tumor that was causing hormone imbalances.

Epithelial elements in superficial angiomyxomas are non-neoplastic growths mimicking embryogenesis.

The man has a genetic skin condition called pachyonychia congenita.

Basal cell carcinoma with matrical differentiation is a rare type linked to hair follicles, with .-catenin important for its development.

Nevus comedonicus is a rare skin condition causing dark bumps, treatable with retinoic acid or surgery.

Cats can have hypersomatotropism without diabetes, suggesting current diagnosis methods may miss cases.

Immune cells boost stem cell activity in hairy moles, causing more hair growth.