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A patient with a nerve disorder died from infection complications after developing insulin resistance from a treatment.

Plica neuropathica is a tangled hair condition that may be caused by hair damage or psychiatric issues and is treated by cutting the hair and addressing mental health.

Non-motor symptoms in myasthenia gravis are common and need early diagnosis for better management.

Severe nutritional deficiency can cause serious health and development issues, including skin problems and hair loss.

A rare skin growth in a baby was successfully removed without coming back.

Selumetinib causes skin and hair side effects in kids with NF1, affecting treatment and quality of life.

Woodhouse-Sakati Syndrome can include unique symptoms like liver issues and low growth hormone.

A man with four autoimmune diseases suggests a new category for multiple autoimmune syndrome.

Patients with both connective tissue disease and acid reflux are more likely to have certain symptoms and physical signs.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

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

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Erosive pustular dermatosis of the scalp can occur about 17 weeks after starting EGFR inhibitors, and early minocycline may help manage it.

A cat with a rare pancreatic tumor and diabetes died despite treatment, showing similar symptoms to a human condition.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Vaccines work well in Netherton syndrome patients, similar to healthy people.

Skin problems are common and important signs of eating disorders and treating the eating disorder can improve these skin conditions.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

A patient's skin rash did not affect the area where a previous viral rash was healing, suggesting a rare immune response.

Nevus comedonicus is a rare skin condition causing dark bumps, treatable with retinoic acid or surgery.

A rare skin condition with cysts was found on a 5-year-old boy's scalp.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Erythema nodosum linked to kerion can be treated effectively with antifungals and steroids to reduce scarring.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

The man has a disease causing skin patches, thickened nerves, and mild muscle weakness.

A 17-year-old girl and her brothers have a rare hair condition with long eyelashes, thick eyebrows, and easily pluckable hair.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

Most skin conditions in Down syndrome are benign and involve dry or thickened skin.