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Masculinization in affected individuals occurs gradually after puberty due to hormone changes.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

JAK inhibitors helped treat hair loss in two people with Down syndrome.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Biotinidase deficiency can be easily diagnosed and treated with biotin to prevent serious harm.

Prednisone treatment helped a woman with Cronkhite-Canada syndrome recover from hair loss and digestive issues.

MCPIP1 in myeloid cells is important for skin cancer development and healthy hair growth.

AMT may cause hair loss and changing dWAT activity could help treat it.

Lack of cystatin M/E causes thin hair and dry skin.

A 6-year-old girl's inability to grow her hair long was due to Loose Anagen Hair Syndrome, which causes hair to shed easily and may improve with age.

A woman with childhood growth hormone deficiency had multiple hormone deficiencies and developed serious lung and kidney problems later in life.

Different skin diseases show unique patterns of skin cell separation, cell death, and granular layer changes.

Obesity and certain hormone levels can lead to advanced bone age in young girls with early breast development.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

MPZL3 protein helps control the size of oil glands and the growth of oil-producing cells in both mice and humans.

DM and AA may share a common cause.

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

Fibrosing alopecia in a pattern distribution is a unique hair loss condition that may respond to antiandrogen therapy.

A 16-year-old boy's alopecia areata progressed unusually to resemble male pattern baldness.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Pseudopelade of Brocq is hard to diagnose and treat, with limited effective options.

The ZIP13 variant is linked to abnormal hair quality.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

A toddler with a rash and developmental delays improved after treatment for severe malnutrition caused by a diet lacking in protein.

Calcium supplements improved bone deformities but not skin papules or hair loss.

A woman with dermatomyositis improved after treatment for neck panniculitis, suggesting similar treatment for related conditions.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

People with mycosis fungoides/Sézary syndrome have a much lower quality of life.