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The document is a detailed medical reference on skin and genetic disorders.

A 5-year-old girl with a rare skin disorder was effectively treated with skin creams instead of oral medication.

A young woman with kidney failure had hair loss due to a common hormonal disorder, which improved with hormone therapy.

Ficus racemosa leaf extracts help heal diabetic wounds and lower blood sugar.

The removed ovarian tumor was a rare type of blood vessel tumor that improved the patient's symptoms and hormone levels after surgery.

Optical Coherence Tomography has potential in diagnosing hair loss and monitoring blood clotting, and could be improved for deeper tissue observation and better hair loss understanding.

Patients with one autoimmune disease should be checked for other autoimmune disorders.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Men with genetic hair loss are more likely to have abnormal blood lipid levels, especially if the hair loss is severe.

Choosing the right model order in brain connectivity analysis can affect the detection of differences between healthy individuals and those with seasonal affective disorder.

Lichen Planopilaris and Frontal Fibrosing Alopecia may help us understand hair follicle stem cell disorders and suggest new treatments.

The mineralocorticoid receptor may play a role in skin and hair health and could be a new target for treating related disorders.

St. John's Wort can cause dangerous high blood pressure if taken with certain foods.

Ovarian SAHA syndrome makes women with PCOS more resistant to insulin and increases their risk of blood sugar problems.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

New method uses hair follicle cells to estimate human body clock phase, potentially improving sleep disorder diagnosis.

Higher lead and cadmium, and lower zinc and iron levels in the blood might be linked to chronic hair loss in women.

Rivaroxaban can cause liver injury, allergic reactions, blood vessel inflammation, and hair loss, but these side effects are rare.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Tofacitinib and ruxolitinib are effective and safe for treating various autoimmune skin and joint disorders.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

Platelet-Rich Plasma (PRP), a protein-rich extract from a patient's blood, shows promise in improving hair density, thickness, and quality, but the best method of use and number of treatments needed for noticeable results are still unclear.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

Media images promote unrealistic beauty standards, affecting body image and eating disorders globally.

Human umbilical cord stem cell vesicles may help treat aging and related diseases.

Recognizing rare causes of MASLD is crucial for effective treatment and preventing complications.

Vitamin C and E may help with certain skin and hair conditions, but more research is needed to confirm their effectiveness.

Dexamethasone can cause diabetes in rats, and Annona muricata bark extract may help lower blood sugar.

Patients with multiple superficial venous thrombosis are at greater risk for serious complications like cancer and recurrent blood clots.