Search

everythinglearnresearchcommunity

for

Search:↓

People with autoimmune skin diseases often have hearing problems and should get their hearing checked early.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

Schimmelpenning Syndrome requires careful evaluation and tailored treatment for skin, eye, and developmental issues.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.

Ultraviolet rays damage hair, smoking may cause hair loss, and good nutrition is important for hair health, but genetics mainly decide hair thickness.

The book details skin conditions in older adults, their link to mental health, cancer treatment importance, hair loss remedies, and managing autoimmune and itchy skin.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Alopecia areata may be linked to hearing problems, so patients should monitor their hearing.

People with alopecia areata often have other health issues like skin diseases, metabolic syndrome, stomach infections, lupus, anemia, thyroid problems, mental health issues, vitamin D deficiency, and hearing and eye problems.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

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

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The document concludes that managing skin conditions during pregnancy is important and requires specialized care.

Follistatin and LIN28B together improve the ability of inner ear cells in mice to regenerate into hearing cells.

A woman poisoned with thallium was successfully treated with activated charcoal and Prussian blue.

Macrophage activation syndrome can be a deadly first sign of systemic lupus erythematosus.

KCNQ potassium channels help control the sensitivity of touch receptors in the skin.

Satoyoshi syndrome can cause eye problems like uveitis and retinal vein issues.

Using skin stem cells and certain molecules might lead to scar-free skin healing.

Pannexin 3 is important for bone formation and the development of bone cells.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

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.

A girl with symptoms like an autoimmune disorder actually had HIV and a fungal infection, which was hard to diagnose and treat, leading to her death.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Social media data can help track and predict COVID-19 symptoms and trends.