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Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Nilotinib can cause generalized keratosis pilaris.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

Shock can be an early sign of Autoimmune Polyendocrine Syndrome Type II.

Eruptive vellus hair cysts are often missed in diagnoses.

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

A baby had a rare case of widespread milia, which was treated and is being monitored.

A 16-year-old boy's arm hair grew more after wearing a splint, but it returned to normal in 8 months.

Different sebaceous gland diseases can be treated with medications, hormone therapy, or surgical methods.

Androgenetic alopecia is linked to heart disease, metabolic issues, and mental health problems.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Acne can't be cured but can be managed with treatments like benzoyl peroxide and diet changes; it's costly and can lead to scarring and mental health issues.

Growth hormone levels affect hair growth and loss, with too much causing excess hair and too little leading to hair loss.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

A 66-year-old woman with skin lesions and other symptoms improved after treatment for porphyria cutanea tarda.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The document concludes that managing Dunnigan-Type Familial Partial Lipodystrophy involves treating associated health issues and using medications like metformin and leptin replacement.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

Hormonal imbalances in Polycystic Ovarian Syndrome (PCOS) might trigger a rare skin disorder called Confluent and Reticulated Papillomatosis (CRP), so dermatologists should consider checking for PCOS in CRP patients.

Recognizing scalp symptoms in PRP is crucial for proper diagnosis and treatment.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Botulinum Neurotoxin-A can treat acne, oily skin, rosacea, hair loss, prevent scars, relieve nerve pain, reduce excessive sweating, and manage psoriasis, but more trials are needed to confirm its effectiveness.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

Dihydrotestosterone and 5α-Reductase play a role in hair loss and prostate health, and finasteride can increase hair growth in men without affecting sperm production, but it doesn't work for postmenopausal women with hair loss.

Minoxidil treatment can reduce hair shedding, increase hair volume, and even change hair color in patients with loose anagen hair syndrome.

Finasteride caused blisters on hands and feet.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.