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Facial dark spots can be caused by the sun, genetics, makeup, or medicine, and are diagnosed by patient history and skin tests.

Understanding chaos and control mechanisms in disease can improve diagnosis and prediction in medicine.

Early diagnosis and aggressive treatment are crucial for better outcomes in lymphomatoid granulomatosis.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

The anti-ageing treatment market is growing by exploiting fears of ageing with unproven promises, which could harm public trust and genuine science.

New hormonal treatments for enlarged prostate show promise for safer, effective non-surgical options.

The document concludes that fexofenadine reduces inflammation in chronic hives, cholestyramine helps half of pregnant women with itchy rashes, and relaxing incisions are a good alternative in facial surgery for the elderly.

Notch1 signaling is crucial for improving wound healing and skin regeneration by affecting stem cell behavior.

The Edwardian medical campaign linked maternal drinking to infant mortality and national decline, influencing hygiene education and leading to a ban on children under 14 from pubs.

Cellulose nanocrystals are promising for making effective, sustainable sensors for various uses.

Family-based treatment is the best outpatient care for stable teens with anorexia, and more research is needed on medication and treatment effectiveness for young people with eating disorders.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

The safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

Polycystic Ovarian Syndrome is common in overweight urban college girls and may increase the risk of heart and metabolic problems.

PCOS increases the risk of heart disease and type 2 diabetes in women.

Doctors linked maternal drinking to infant mortality and national decline, leading to public awareness and changes in law.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

Citrullinated proteins from Porphyromonas gingivalis may contribute to rheumatoid arthritis.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Enzymes are classified into six types and are essential for many biological processes, with only a few targeted by drugs.

The conclusion is that the best approach for treating Female Pattern Hair Loss is a combination of different treatments.

Cronkhite-Canada Syndrome often leads to death within 6-18 months.

Researchers developed an algorithm for self-diagnosing scalp conditions with high accuracy using smart device-attached microscopes.

Gastroparesis may cause hair loss due to micronutrient deficiencies, and multivitamins might help.

Genetics and hormones cause hair loss; finasteride treats it safely.

Female pattern hair loss treatments vary in effectiveness and may have side effects.

No cure for female pattern hair loss, but various effective treatments exist.

Humans lost body hair relatively recently in evolution.

New biopsy techniques and tools improve alopecia diagnosis, and both too much and too little selenium can cause hair loss.

Doctors often miss Hair Tourniquet Syndrome, which can lead to serious damage if not treated quickly.