Search

everythinglearnresearchcommunity

for

Search:↓

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A woman developed rare, unexplained curly hair on her scalp and eyelashes.

The document concludes that secondary syphilis cases are increasing and often misdiagnosed, pityriasis rubra pilaris can be distinguished from psoriasis by skin cell features, and different skin layers produce specific components during skin repair.

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

Oxidative stress contributes to hair graying and loss as we age.

To diagnose hair loss, use a systematic approach including history, exams, and tests.

Dermoscopy improves diagnosis and treatment monitoring for children's skin infections, inflammations, and hair disorders.

Notch-related genes play a key role in the development and cycling of hair follicles.

Endoglin is crucial for proper hair growth cycles and stem cell activation in mice.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

STAT3 signaling is important for healthy skin and hair follicles, and its disruption can lead to skin conditions like atopic dermatitis.

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

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

Testosterone therapy aims to treat hormone deficiencies and various conditions safely and effectively, but requires careful patient monitoring due to potential side effects.

Doctors should diagnose hair loss by examining the patient and possibly doing tests, and then treat it based on the type, which may prevent permanent hair loss.

The document concludes that skin and nail changes can indicate various underlying health conditions.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Female pattern hair loss is different from male pattern hair loss and has unclear genetic causes.

Men with a family history of hair loss are more likely to experience it themselves, especially if both parents have hair loss.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Botulinum toxin shows promise for various skin conditions but requires more research for confirmation and standardized use.

Accurate diagnosis is key for treating different kinds of hair loss, and immune response variations may affect the condition and treatment results.

Hormone imbalances can cause skin diseases, and understanding these links is important for diagnosis and treatment.

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

Lichen planopilaris causes permanent hair loss and scarring due to damage to hair follicles and can be mistaken for other hair loss conditions.