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A 15-year-old boy's severe scalp condition improved significantly with adalimumab and baricitinib treatment.

A rare scalp condition can occur due to leukemia affecting the skin.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

A rare scalp condition with hair loss was correctly diagnosed and treated, leading to hair regrowth.

Postmenopausal women may experience frontal hairline and eyebrow loss due to cicatricial fibrosis.

RCM and dermoscopy help identify different types of hair loss in children.

A new genetic variant of Woodhouse-Sakati syndrome was found in two adult sisters in Russia.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

Early diagnosis and treatment of endocrine disorders like HAIR-AN syndrome can improve outcomes in adolescents.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Woman has discoid lupus, frontal fibrosing, and androgenetic alopecia.

A scalp biopsy revealed systemic amyloidosis in a woman who initially seemed to have a common hair loss condition.

A patient with patchy hair loss was successfully treated for Tumid Lupus Erythematosus after other treatments failed.

Some brain cancer cells avoid immune system detection, and certain treatments could target this to slow their growth; also, certain fat cell precursors help regenerate hair and skin after injury.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Thymic LCH may be underdiagnosed, so thymic ultrasound should be considered in infants with cutaneous LCH.

Pseudopelade can affect both the scalp and beard, causing hair loss.

Early diagnosis and treatment can reduce cicatricial alopecia in middle-aged individuals, especially females.

Most hair loss in captive rhesus macaques is likely due to environmental and behavioral factors.

Lichen planopilaris can occur with multiple autoimmune diseases.

A man developed facial skin lesions after a stem cell transplant, which improved with specific treatments.

Trichodysplasia spinulosa can occur after a heart transplant due to immunosuppressive drugs.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

An elderly man's non-healing scalp lesion was successfully treated with a strong topical steroid.

Lupus panniculitis of the scalp causes linear hair loss and needs ongoing treatment to prevent recurrence and lupus.

Upper eyelid hyperpigmentation can help diagnose facial lichen planus pigmentosus in patients with frontal fibrosing alopecia.

A rare benign skin growth called melanocytic matricoma was identified in a 69-year-old man.

Cystic panfolliculoma resembles hair follicle tumors due to specific cell interactions.

Acitretin moderately improved skin and eye issues but not hair loss or light sensitivity in a 3-year-old with IFAP syndrome.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.