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Injecting triamcinolone into the eyebrow area may help eyelash regrowth in alopecia areata patients.

A child with rickets and hair loss might have a rare type of rickets that doesn't improve much with usual vitamin D and calcium treatment.

Hypothyroidism harms rat skin, but topical triiodothyronine may help improve it.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Brandt syndrome, with symptoms like skin rash, hair loss, and diarrhea, improves quickly with zinc supplements.

The conclusion is that normal trace element levels in newborn calves' hair are between the 25th and 75th percentiles, and levels outside this may indicate diselementosis.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

Beta-blockers and anti-anginal medications have various side effects and interactions that require careful monitoring and individualized treatment.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

Eating disorders like anorexia and bulimia cause skin problems, and dermatologists can help detect these disorders early for better treatment outcomes.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Zinc deficiency in children can cause skin issues and can be serious if not diagnosed and treated properly.

The document concludes that targeting the androgen receptor may be a promising breast cancer treatment, especially for certain types.

Chemotherapy and bone marrow transplant can cause permanent hair loss.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

The study found that certain microRNAs are higher in the cells and lower in the fluid of women with a specific type of polycystic ovary syndrome, and one microRNA could potentially help diagnose the condition.

Anorexia nervosa can cause skin problems, which may help with early diagnosis and usually improve with treatment.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Most Korean systemic lupus erythematosus patients experienced hair loss, often as non-scarring diffuse hair loss, with non-scarring patch alopecia also common.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

The androgen receptor is a promising target for breast cancer treatment, especially in triple-negative cases, but more research is needed for personalized therapies.

Stress affects skin health and emotional well-being should be considered in skin disease treatment.

A patient with Satoyoshi syndrome improved with a treatment combining several medications, including carbamazepine and methotrexate.

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

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.