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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.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

Androgens and androgen receptors are important for metabolic health, affecting how the body uses glucose and fats through mitochondrial function.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

Different races and genders have unique skin and hair issues, requiring specialized care and more research for effective treatment.

Ice-skating athletes often have skin problems due to cold, infections, and inflammation, needing careful treatment and prevention.

PCOS in lean women is a serious health condition with implications beyond fertility, affecting metabolism and increasing cardiovascular disease risk.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

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

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

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

Lipedema is a painful fat disorder in women that's hard to treat, often worsens with hormonal changes, and requires symptom-focused therapies.

Minoxidil improved hair growth in a child with a rare genetic disorder.

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.

Visible light can damage skin and most sunscreens don't block it well; more research is needed on its effects and protection methods.

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

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Dupilumab helped improve skin and prevent new lesions in a child with a rare immune disorder and severe eczema.

Only a few hair-specific keratins are linked to inherited hair disorders.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Gastric bypass surgery improved a woman's hormonal disorder without the need for medication.