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Living with metastatic pancreatic cancer involves symptoms like fatigue and nausea, and impacts like anxiety and reduced physical function.

Two patients treated with TAC for mouth fibrosis improved but developed Cushing's Syndrome symptoms.

CRPS I is complex, linked to immune and nerve issues, and needs comprehensive treatment.

Pegylated interferon-alpha 2a can cause a rare nerve disorder, but early treatment can lead to full recovery.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

A woman was diagnosed with Sheehan's syndrome and a rare complication of diabetes insipidus 33 years after symptoms began, improving with hormone therapy.

A woman's scalp condition improved with specific ointment after a hair piece caused skin issues.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Cantú syndrome may be linked to pituitary adenomas.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

Tattoos may trigger autoimmune symptoms in some people.

A hidden autoimmune syndrome was found during a shock, showing thyroid, adrenal, and ovarian issues.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Fatigue is the most common symptom in both ongoing symptomatic COVID-19 and post-COVID-19 syndrome.

A baby with KID syndrome died from infections and organ failure at 18 months old.

Post-drug syndromes are often overlooked, and better systems and education are needed to improve drug safety.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Post-finasteride syndrome causes lasting sexual, neurological, and physical side effects in some people after taking finasteride.

EPDS and MS might share an immune-related cause.

Metabolic syndrome's individual issues are real and need treatment to reduce diabetes and heart disease risks.

Alopecia Areata causes emotional stress and stigma, but those with severe hair loss may adapt better.

Autoimmune polyglandular syndrome can cause temporary brain issues that may improve on their own.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Thyroid hormone therapy effectively treated the man's rare muscle and heart issues.

There might be a skin condition related to COVID-19.