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Two boys developed a viral skin infection during chemotherapy, which resolved with improved immune function.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

LIPH mutations cause woolly hair in some Chinese people.

Genetic analysis is crucial for diagnosing ectodermal dysplasia syndromes, and new therapies may help improve skin issues.

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

Three white adults had a rare scalp condition with increased fat and sometimes hair loss, suggesting it's not limited to black women and might be more widespread.

Women with PCOS have higher cardiometabolic risks.

The hair coat disorder in Schipperkes is similar to Alopecia X and involves increased androstenedione levels and hair cycle arrest.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Different types of PCOS have different levels of metabolic problems, with the most severe type showing the highest disturbances.

A high fat lard diet may protect against skin fibrosis and affect hair growth.

Para-aminobenzoic acid in hair supplements can cause autoimmune hepatitis.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

People with hair loss have worse cholesterol levels, possibly linking hair loss to heart problems.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Women with PCOS have different levels of certain fats and proteins in their blood, which could help diagnose the condition.

The patient with lupus and Degos' disease showed significant improvement with treatment.

The conclusion is that managing cholesterol is important for women, especially during pregnancy, breastfeeding, and with PCOS, and involves regular screening and careful treatment choices.

The patient was diagnosed with anorexia nervosa and severe malnutrition, requiring urgent refeeding and monitoring.

The newborn was diagnosed with a rare skin disorder causing blisters, which requires careful wound care and family support.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Epidermolysis bullosa is an inherited condition causing fragile skin with no cure, managed by wound care and experimental treatments show promise.

Most patients with autoimmune blistering diseases experienced some hair loss, which may be underreported and linked to disease severity.

Peginterferon alpha-2a effectively treats acute hepatitis C in hemodialysed patients, despite some side effects.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

People with severe acne tend to have higher levels of betatrophin.

Selenium deficiency can cause skin and hair color loss, muscle weakness, and blood cell changes, but these improve with selenium supplements.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.