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Temporal triangular alopecia in infants is mostly seen in males at birth, with unique features that help with diagnosis.

Most inconsolable crying in infants is not due to a serious cause, and a detailed check-up is typically enough to find the reason.

Skin biopsies are recommended for confirming alopecia diagnosis due to variability in clinical assessments; the link between vitamin D levels and alopecia is unclear.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

The document suggests a personalized treatment plan for alopecia areata based on the patient's age and hair loss severity, using a range of therapies ranked by effectiveness and safety.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Hair damage shows as fragility, dullness, and discoloration, varies by ethnicity, and is worsened by cosmetic procedures and diseases.

Chronic telogen effluvium may not be a unique condition and could be confused with other types of hair loss.

Resveratrol improved hormone levels, menstrual cycles, hair loss, and ovarian function in PCOS patients.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Alopecic and aseptic nodules of the scalp are rare, treatable, and often resolve with doxycycline or on their own.

New melanoma treatments can cause skin side effects, including skin cancer and rashes, but combining treatments may reduce these risks.

Mycophenolate mofetil can effectively treat autoimmune hepatitis when standard drugs fail.

Taking Propecia might lead to the development of cataracts.

Early diagnosis and quick treatment are crucial for severe lupus cases.

Cyclophosphamide often causes gastrointestinal issues, hair loss, and low blood cell counts in Chinese patients with autoimmune diseases.

Women with hair loss had higher levels of certain hormones, suggesting a link to a condition like PCOS.

The document concludes that while there are various treatments for Alopecia Areata, there is no cure, and individualized treatment plans are essential due to varying effectiveness.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Severe Hidradenitis Suppurativa increases missed and unproductive workdays.

Abrocitinib at 100 mg and 200 mg daily may significantly improve moderate-to-severe atopic dermatitis in patients 12 years and older.

Using a patient's own fat tissue helped treat hair loss caused by an injury.

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

The book "Dermatology" has useful content but some sections lack detail and accuracy; it's recommended for dermatologists to review before buying.

Iron infusions can help improve hair loss in patients who can't take oral iron supplements.

Biodegradable microneedle patches help topical steroids work better for prurigo nodularis.

Bimatoprost is safe and improves eyelash growth in healthy kids but not in those with eyelash loss from chemotherapy or alopecia.

Hypothyroidism may cause certain types of hair loss.