Search

everythinglearnresearchcommunity

for

Search:↓

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

Combining genetic and physical data improves diagnosis and treatment for early-onset monogenic diabetes.

A woman's hair loss was due to trichotillomania, which is often misdiagnosed and can require different treatments based on age and underlying conditions.

Leflunomide successfully treated a rare skin condition in a liver transplant patient.

A man developed severe skin reactions after using a treatment for hair loss.

Trichodynia is a painful scalp condition linked to hair loss and mental health issues, with limited treatment options.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

Valproic Acid could potentially be used to treat immune-related conditions due to its ability to modify immune cell functions.

Children with frequent severe infections and low antibodies should be checked for immune deficiencies.

There may be a link between Helicobacter pylori infection and the skin condition pityriasis versicolor.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.

The man had pretibial myxedema and hyperthyroidism, causing skin changes and thyroid issues.

Machine learning identified three unique subtypes of androgen excess in women with PCOS, each with different metabolic risks.

Pentoxifylline effectively improves pretibial pruritic papular dermatitis.

Mycophenolate mofetil helped reduce steroid use in treating a dog's autoimmune skin disease.

Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.

A woman with PCOS successfully overcame secondary infertility and became pregnant with triplets after treatment.

Large databases in research can lead to misleading conclusions due to biases and chance findings; researchers should analyze data more rigorously.

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

Early diagnosis and haemodialysis can effectively treat thallium poisoning.

Cronkhite-Canada syndrome is a rare condition causing gut polyps, hair loss, skin changes, and nail issues, often with a poor outlook.

A patient with granuloma annulare experienced both isotopic and isomorphic responses, with skin lesions responding to steroids but relapsing after stopping treatment.

Some people's hair loss is caused by multiple factors, with the most common being a mix of AGA and CCCA.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Most patients with dermatomyositis had skin rash and were treated with prednisolone and hydroxychloroquine.

Polygoni Cuspidati Rhizoma et Radix contains compounds that inhibit certain enzymes.

Hairpulling, skin picking, and nail biting cause significant harm and need more research for better treatments.