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The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

The document explains the genetic causes and characteristics of inherited hair disorders.

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

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

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.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

Experts discussed treatments for skin conditions in children, emphasizing hydration, cautious medication use, and early intervention for infections.

Epidermal stem cells could lead to new treatments for skin and hair disorders.

Certain signals and genes play a key role in hair growth and regeneration, and understanding these could lead to new treatments for skin regeneration.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Topical treatments can deliver active molecules to skin stem cells, potentially helping treat skin and hair disorders, including skin cancers and hair loss.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

Pregnant women with Systemic Lupus Erythematosus have a higher risk of blood clotting problems.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

A boy with a rare skin condition improved quickly after starting zinc supplements.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

AGA causes hair loss by shrinking hair follicles due to DHT binding, and can be treated with finasteride and minoxidil.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

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

RAPK is a rare skin disorder with pigmented spots, mainly on hands and feet, starting in youth.

Insulin resistance may contribute to various skin diseases and treating it could improve skin health and prevent more serious conditions.

Loose Anagen Syndrome causes easy-to-pull, thin hair, mainly in young girls, and improves with age.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

EF and PXE not closely related.

A man's chest hair turned white after a shingles infection, possibly due to virus-damaged pigment cells.

Cytochrome P-450 enzymes in the skin help break down various substances and could be targeted to treat skin conditions.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.