Search

everythinglearnresearchcommunity

for

Search:↓

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

Using neurohormones to control keratin can lead to new skin disease treatments.

Lysophosphatidic acid is important for skin health and disease, and could be a target for new skin disorder treatments.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

Early diagnosis and treatment, like topical minoxidil, can prevent hair loss in children.

Different hair loss types need accurate diagnosis for proper treatment.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

Dentists should start preventive treatments early for children with Ichthyosis Vulgaris to avoid dental problems.

The document concludes that proper recognition and treatment of skin appendage disorders are important for management.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Terbinafine is more effective than itraconazole for toenail fungus, especially in older patients, and debridement improves its effectiveness.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

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

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

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

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

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.

Six genetic conditions are often linked to complete scalp hair loss in children.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Hair follicles are essential for skin health, aiding in hair growth, wound healing, and immune function.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.