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COVID-19 vaccination may be linked to MIS-C in children, highlighting the need for quick diagnosis and treatment.

Myasthenia gravis can affect both motor and non-motor systems due to immune system issues.

An antibiotic called co-trimoxazole can effectively treat autoimmune diseases.

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

Trichobezoars can cause serious health issues like biliary obstruction, and treatment includes surgery and therapy to prevent recurrence.

Early diagnosis of pseudopelade of Brocq in men is crucial to prevent permanent hair loss.

Anti-epileptic drugs may cause visual and hair side effects due to enzyme inhibition, especially in genetically predisposed individuals.

A woman with systemic sclerosis developed a unique scarring hair loss combining features of systemic sclerosis and frontal fibrosing alopecia.

PRP therapy can temporarily grow hair in CCCA patients but isn't a permanent cure.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Two siblings have a rare hair condition caused by a new genetic variant.

Dupilumab helped a 4-year-old grow hair back after another treatment failed.

The article concludes that careful examination is crucial for the timely diagnosis and treatment of a rare scalp condition in an Aboriginal Canadian teenager.

Recognizing and treating overlap syndrome in connective tissue diseases is crucial.

Two siblings have a rare genetic condition causing curly, coarse hair.

Early biotin treatment can reverse symptoms of congenital biotinidase deficiency.

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

COVID-19 can cause hair to become progressively kinked.

A patient with "strawberry gingivitis" improved after correct treatment for Granulomatosis with polyangiitis, highlighting the need for early diagnosis.

Posterior column injuries are common in tibial plateau fractures, and CT imaging is crucial for accurate treatment planning.

A rare skin condition usually found near the eyes was found on a farmer's scalp.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Levetiracetam is widely used and generally well-tolerated for treating idiopathic generalized epilepsies, with tiredness as the main side effect.

A woman developed a skin condition called Pemphigus Vulgaris after a treatment to help with hair loss.

A man developed recurring scalp inflammation and hair loss after a head injury.

Lupus erythematosus panniculitis on the scalp can cause unique geometric hair loss patterns.

Two siblings stayed rickets-free for 14 years after stopping treatment.

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