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Zinc supplements improved symptoms in a Uyghur infant with a rare genetic disorder affecting zinc absorption.

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

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Leukemia can sometimes appear as unusual skin issues in children.

A woman was diagnosed with a rare adrenal gland cancer that did not show usual hormone-related symptoms.

Prednisolone improved symptoms in a woman with Cronkhite-Canada syndrome, but regular screenings are needed due to cancer risk.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Most children with childhood-onset lupus in Baghdad responded well to treatment, but some developed chronic kidney disease or died.

New mutations in the DSG4 gene cause a rare hair condition.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Leflunomide and anthralin may effectively treat severe alopecia areata.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

The man was diagnosed with stage III multiple myeloma and treated to improve kidney function.

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

A 93-year-old woman developed a rare scalp condition after therapy, which improved with steroids, not antibiotics.

Adalimumab helped control a child's severe eye disease when other treatments failed.

Alopecia areata has different forms and can significantly affect quality of life, especially in more severe cases.

Linear Discoid Lupus Erythematosus of the scalp can cause hair loss and should be considered in similar cases.

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

Systemic corticosteroids might help treat hair loss caused by alemtuzumab in MS patients.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

A genetic marker linked to a type of hair loss was found in most patients studied.

Certain genetic variations can make people more likely to experience hair loss and low white blood cell count from azathioprine.

Genetic defects in androgen production are linked to male developmental disorders and are improving treatment understanding.

Early diagnosis and lifelong zinc supplementation are crucial for treating acrodermatitis enteropathica effectively.

Monilethrix is a rare genetic hair disorder that's hard to treat.

Monitor for early signs of azathioprine toxicity and check blood counts regularly.