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Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

A child had a rare case of scarring hair loss with skin disease, which is hard to treat and stressful.

Tight hairstyles can cause a rare scalp condition with thick skin folds.

The study found that white hair in vitiligo has specific patterns and structures, which vary with the stage of the disease and may be similar to another hair condition.

A woman with subacute cutaneous lupus erythematosus had widespread skin symptoms triggered by medication and sunlight, which improved with specific treatments.

An 80-year-old woman with Cronkhite-Canada syndrome had multiple polyps and symptoms like diarrhea, hair loss, nail issues, and dark skin.

Congenital atrichia is a rare condition where children are born without hair, and treatment is often ineffective.

Southern Chinese women with female pattern hair loss have less, thinner hair and smaller hair follicles.

CP-690,550 significantly reduced itching in patients with moderate-to-severe plaque psoriasis.

The letter suggests that psychiatric issues, not a sleep disorder, were likely the cause of a patient's self-inflicted leg ulcers.

The patient had paraneoplastic pemphigus without mucosal involvement.

A mother and daughter had severe skin, hair, and eye issues linked to IFAP.

A rare form of lupus can cause severe nerve damage and other symptoms, but treatment can help.

IgG4-related disease can cause scalp hair loss that looks like acne keloidalis nuchae.

The rash on the infant indicated a serious underlying condition.

Lichen planopilaris is a chronic, scarring hair loss condition with no definitive cure, requiring accurate diagnosis and treatment to manage symptoms.

Topical steroids can manage chronic scalp pustules in elderly women.

Recognizing eyebrow hair loss linked to a rare skin condition is crucial for proper treatment.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Shiny white structures in trichoscopy can indicate long-standing discoid lupus erythematosus alopecia.

Trichotillomania in children is a sign of emotional distress needing tailored treatment and family support.

Clq deficiency is linked to systemic lupus erythematosus symptoms.

MCTD should be considered in children with recurring muscle issues, lupus-like symptoms, and edema.

A boy with long QT syndrome was treated successfully, highlighting the need for careful evaluation of chest pain in children for heart conditions like LQTS.

The Gillies temporal incision is a safer and more cosmetically appealing method for biopsy of the superficial temporal artery.

The patient improved after antiviral treatment for a viral infection.

Early genetic testing and zinc therapy are crucial for managing acrodermatitis enteropathica in infants.

PTCH gene mutations contribute to basal cell carcinoma development.