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Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

A man developed a rash similar to pityriasis rubra pilaris after starting sorafenib for cancer, possibly due to the drug's effect on skin cells.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A unique type of lupus panniculitis causes reversible hair loss on the scalp in East Asians.

A kidney transplant patient developed pink skin bumps with spiny centers on her face and limbs.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

A young woman with visual issues and other symptoms was diagnosed with lupus and antiphospholipid syndrome, and improved with treatment.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

A rare skin condition caused scarring hair loss on the scalp.

A man developed a rare skin condition and drug-induced lupus, highlighting the need for biopsy in diagnosing skin issues caused by sunlight.

Visual field defects in lupus nephritis can be caused by hypertensive retinopathy, not glaucoma or medication toxicity.

Systemic lupus erythematosus is an autoimmune disease causing diverse symptoms and major organ involvement.

Using Janus kinase inhibitors (JAKi) in COVID-19 treatment requires careful consideration due to their immunosuppressive effects.

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

RHUPUS should be considered in children with deforming arthritis.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Renal transplant patients on tacrolimus and sirolimus may develop acne keloidalis nuchae.

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

A 19-year-old man had a rare skin condition on one side of his face that looked like another skin disease.

A Japanese man with rare skin conditions improved with hydroxychloroquine treatment.

The patient improved after antiviral treatment for a viral infection.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

Tofacitinib significantly improved symptoms in a patient with overlapping autoimmune disorders.

A child with Sweet syndrome was found to have chronic granulomatous disease and improved with treatment.