Search

everythinglearnresearchcommunity

for

Search:↓

Topical squaric acid dibutylester worsened discoid lupus erythematosus in a patient.

Chinese patients with systemic lupus erythematosus commonly experience oral ulcers, arthritis, alopecia, skin rash, and nephritis.

Metformin and liraglutide improved symptoms of HAIR-AN syndrome in a child.

Increased HIF-1α is linked to the inflammation and severity of hidradenitis suppurativa, suggesting treatments that lower HIF-1α could help.

Mogamulizumab can cause hair loss and skin rashes.

Long COVID causes lasting symptoms and needs ongoing care.

An old recipe called "Champigny Saumure" might help treat a rare scalp condition.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Cronkhite-Canada syndrome causes chronic diarrhea and has a poor prognosis despite treatment.

A patient with Myotonic dystrophy type 1 had multiple tongue hemangiomas and was sensitive to anesthesia.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

A woman in Pakistan was diagnosed with Lupus Vasculitis and treated successfully.

Panchkarma treatment can help manage symptoms of Systemic Lupus Erythematous.

Brandt syndrome, with symptoms like skin rash, hair loss, and diarrhea, improves quickly with zinc supplements.

Chronic granulomatous disease may be linked to developing systemic lupus erythematosus.

RCVS should be considered in thunderclap headaches, and MRA and DSA are better for diagnosis than CT angiogram.

A boy with long QT syndrome was treated successfully, highlighting the need for careful evaluation of chest pain in children for heart conditions like LQTS.

A woman with Degos disease managed her condition for nine years with medications and had two healthy pregnancies, while a separate finding suggests a possible link between female pattern hair loss and high blood pressure.

Rhupus is a complex syndrome that is hard to diagnose due to unclear clinical criteria.

Long COVID affects over half of COVID-19 survivors, causing a range of symptoms like fatigue and neurological issues, with no specific treatment yet.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A woman with lupus had right heart failure due to blood clots in her lungs, but treatment improved her condition.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.