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A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

Human body follicles have diverse structures and functions important for health.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

The outer root sheath in hair follicles changes during growth, with different keratinization processes in its layers.

Reactive lipids from aging cells change the extracellular matrix, affecting cell function and inflammation.

Immature hair cells can grow and change into different types of hair cells over time.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

The naked mutation in mice causes hair loss and helps identify keratin genes.

Onychomatricoma is a unique nail tumor that mimics the entire nail unit and is not related to other hair-related tumors.

Calcium fatty acid deposits found in human hair can change its appearance and feel.

An 87-year-old man showed unusual signs of Hodgkin lymphoma, primarily high calcium levels, which improved after treatment and revealed the disease.

Bubble hair deformity may be caused by hair shaft trauma and can improve with gentle hair care.

Becker's Melanosis and Hypertrichosis mainly affects young males, causing brown skin patches and extra hair on one side of the upper body.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Cholesterol and phospholipids increase in mouse skin during cancer development, with differences between male and female skin.

Fibroblast spheres can form stem cells, but marker distribution needs more study.

Thymoma in cats can cause hair loss without inflammation.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

A man had a non-cancerous, fast-growing skin lump on his arm that was removed with surgery.

Hair follicle hyperplasia is common in both benign and malignant skin lymphoproliferative disorders, with a proposed new term "pseudolymphomatous adnexitis."

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.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Punctate follicular porokeratosis is a skin condition with specific features seen in hair follicles.