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SLE patients often face depression and anxiety due to physical changes, with African-American and Hispanic patients having higher unmet psychological needs.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Some people in Saudi Arabia experienced hair loss after the COVID-19 vaccine, more often in women and those without prior hair loss.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.

Intense pulsed light is a safe and effective way to thin hair for East Asians after hairline surgery.

Lipedema is a painful fat disorder in women that's hard to treat, often worsens with hormonal changes, and requires symptom-focused therapies.

Using camphorated and mentholated chlorophenol in dental treatments can lead to severe gastrointestinal issues and hair and nail loss.

Managing severe infections in SLE patients requires tailored treatment strategies.

A 46-year-old man showed symptoms of a rare condition usually seen in postmenopausal women, highlighting the need for dentist-dermatologist collaboration.

A specific gene mutation causes Olmsted syndrome.

Cyclosporine-A can cause serious blood clots in the brain, so patients need careful monitoring.

Systemic lupus erythematosus treatment can restore vision in patients with retinal artery occlusion.

A child with a rare vitamin D-resistant condition improved with treatment.

Surgical robots have improved but still can't perform tasks or make decisions on their own.

The document concludes that a systematic approach is crucial to identify causes of androgen excess in women beyond the most common cause, Polycystic ovary syndrome (PCOS).

The true incidence of post-Finasteride syndrome is unclear, and more research is needed.

Retinoids are effective for various skin conditions and hair loss but have serious side effects, so low doses are recommended.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

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.

PBMCsec can help reduce and improve thick skin scars.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Rehabilitation therapy helped a severe COVID-19 patient regain muscle mass and return to normal life.

Young adults who had liver disease as children often experience significant health problems and frequently need transplants.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Early diagnosis and aggressive treatment are crucial for managing SLE-related pancreatitis in children.

New ginseng compounds may help treat degenerative diseases.

The FAW-FS algorithm improves depression recognition, and psychological interventions help AGA patients' mental health.

Keratinocytes and adipose-derived stem cells can effectively heal difficult skin wounds.

The first pediatric case of naevus trichilemmocysticus was documented.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.