Search

everythinglearnresearchcommunity

for

Search:↓

Most Korean systemic lupus erythematosus patients experienced hair loss, often as non-scarring diffuse hair loss, with non-scarring patch alopecia also common.

People with mycosis fungoides/Sézary syndrome have a much lower quality of life.

Myhre syndrome symptoms worsen over time, with specific genetic variants affecting severity.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

Accurate diagnosis of SLE requires extensive testing due to its complex symptoms.

Scurvy, caused by lack of vitamin C, can be mistaken for other conditions but improves with vitamin C supplements.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

A woman with Lupus Vasculitis improved after treatment with steroids and other medications.

Hydroxychloroquine helped improve scleromyxoedema in patients, but caused side effects in some.

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

Syphilis treatment resolved hair loss and eye symptoms, highlighting its importance in diagnosing unusual alopecia.

A new genetic variant of Woodhouse-Sakati syndrome was found in two adult sisters in Russia.

Repeated biopsies are crucial for managing lupus panniculitis when initial treatments fail.

Two children with lysinuric protein intolerance showed symptoms similar to lupus.

People with psoriasis have more health problems, including autoimmune diseases, than those without it.

Testing for various autoantibodies in Indian children with lupus can help predict disease symptoms and risks.

Some medications can improve skin conditions, while lifestyle factors like smoking and drinking may worsen them; treatments like monoclonal antibodies and imiquimod cream show promise for certain skin diseases.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Parry–Romberg Syndrome can involve the brain even without obvious symptoms, and a new diagnostic framework is suggested for early detection.

A 60-year-old man with Cronkhite-Canada syndrome improved with treatment, but the condition has a high mortality rate and a risk of colorectal cancer.

High-dose corticosteroid treatment helped improve symptoms in a patient with Adult Onset Still Disease.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

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

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Fibromyalgia slightly more common in SLE patients but doesn't affect SLE activity assessments.

Taste disorders in Cronkhite-Canada syndrome are severe in the front of the tongue but improve with treatment.

GLPLS is a rare skin condition with specific hair loss and skin symptoms.

Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.