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Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

A cat lost hair on its back a month after a road accident, despite no initial skin injuries.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

The authors suggest standardizing how the heart's electrical axis is calculated to improve precision and consistency in ECG analysis.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

An elderly man with skin amyloidosis and abnormal blood proteins was monitored without finding widespread disease after 18 months.

A boy on a ketogenic diet and anti-epileptic drugs developed skin issues due to stopping vitamin supplements, which improved with proper supplementation.

Low-dose oral minoxidil is a promising, safe treatment for various hair diseases, improving hair thickness and density, but more research is needed on long-term side effects and treatment duration.

Meis2 is essential for touch sensation and nerve function in mice.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Most vitiligo patients in Makkah are young women, often with family history and thyroid issues.

A Shi Tzu dog with high cortisol levels improved after increasing the dose of trilostane.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Mice that can regenerate tissue have cells that pause in the cell cycle, which is important for healing, similar to axolotls.

A woman's shingles infection triggered her first episode of a rare neurological disorder and blood vessel inflammation.

The document discusses hair and nail conditions, updates on treatments for alopecia, and controversies around finasteride use.

A multidisciplinary approach is crucial for treating complex cases of Rapunzel syndrome in children.

The transcription factor Meis2 is essential for touch sensation and proper nerve development in touch receptors.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Repeated biopsies are crucial for managing lupus panniculitis when initial treatments fail.

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

The document concludes that hair loss in cats is caused by various factors, including allergies, mites, infections, and hormonal issues, with treatments varying accordingly.

Caffeic acid helps protect rats from the harmful effects of acrylamide.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

Lentiginous melanoma is most common on the face, especially the nose, cheek, and pre-auricular areas, with men more likely to have it on the scalp, ears, upper back, and trapezius, and women on the cheek and anterior arm. Sun damage is a key factor in its formation.

The cancer drugs bortezomib and lenalidomide cause skin side effects in many patients.

Obesity leads to physical, metabolic, reproductive issues, higher healthcare costs, and mental health problems.

Dupilumab can improve both atopic dermatitis and alopecia universalis.