Search

everythinglearnresearchcommunity

for

Search:↓

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

The guidelines suggest using various treatments, including antidepressants and steroids, for alopecia areata and discuss the condition's genetic and immune aspects.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.

Alopecia areata causes sudden hair loss, has genetic links, and can be managed but not cured.

The document concludes that PCOS is a complex disorder caused by both genetic and environmental factors, affecting women's health in various ways, and requires personalized treatment.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Female pattern hair loss is common, worsens with age, and requires long-term treatment to manage.

The document says how to diagnose and treat hair loss from alopecia areata, but there's no cure and treatments vary.

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

Machine learning and deep learning can effectively diagnose alopecia areata.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

Hair color is influenced by genetics and can indicate certain health conditions.

Female pattern hair loss involves hormonal factors, genetics, and may be linked to low ferritin levels.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

New treatments are being explored to slow or reverse hereditary hair loss.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

Hair loss is caused by genetics and hormones, diagnosed through examination and biopsy, and treated with medications or surgery.

People with Down syndrome are more likely to experience hair loss, and using dermoscopy can help diagnose it.

New insights into the causes and treatments for the autoimmune hair loss condition Alopecia areata have been made.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

The document suggests finding a simpler, cheaper way to diagnose Uncombable Hair Syndrome.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

Recent progress has been made in understanding inherited hair and nail disorders.