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Using tissue expanders for scalp reconstruction in patients with extensive Aplasia Cutis Congenita is effective and has minimal complications.

Pharmacists should interpret lab data and perform physical exams to improve patient care.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

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.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

Acne is caused by genetics, diet, hormones, and bacteria, with treatments not yet curative.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

Understanding how acne develops in different diseases could lead to new treatments.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Scientists created a tiny, 3D model of a hair follicle that grows and acts like a real one.

Studying acne-related syndromes helps us understand acne causes and can lead to new treatments.

Hormones, especially androgens, play a key role in acne, which can be a symptom of systemic diseases like PCOS and may require targeted treatment.

Acne is a chronic disease linked to various systemic conditions and has significant psychological and social effects.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

CaV1.2 helps activate hair follicle stem cells without calcium flux.

A 23-year-old woman's missed periods were caused by a rare genetic disorder treated with hormone patches.

The 18-year-old girl likely has a condition called müllerian agenesis, which caused her to not have a uterus and experience no menstrual periods.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Laminin-511 is crucial for early hair growth and maintaining important hair development signals.

The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.

Anti-acne medications may work by reducing the activity of a protein involved in acne development.