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A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Lipedema is a painful fat disorder in women that's hard to treat, often worsens with hormonal changes, and requires symptom-focused therapies.

A rare skin growth was successfully removed without recurrence after one year.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Dermoscopy helps diagnose and monitor treatment for hair loss from scarring conditions like discoid lupus and lichen planopilaris.

Both environmental and genetic factors contribute to Lichen Planopilaris.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

A man's skin condition, pemphigus vulgaris, came back after he was treated with interleukin 2 for cancer.

Mitochondrial dysfunction and oxidative stress may play a role in Lichen Planopilaris.

A man with a type of skin lymphoma had unusual yellowish skin growths despite normal blood lipid levels, and treatment reduced some symptoms but not the growths.

The conclusion is that Erosive Pustular Dermatosis of the Scalp is a rare condition best treated with strong topical steroids and sometimes systemic treatment.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

Skin problems are common in lupus patients and should be treated early to prevent worsening.

The patient's symptoms improved with treatment but recurred when the steroid dose was reduced, requiring ongoing therapy.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

Lichen simplex chronicus on the scalp can be diagnosed by specific hair and skin signs and treated with corticosteroids and therapy.

Long eyelashes in a patient were an unusual sign of systemic lupus erythematosus.

Biopsy is crucial for accurately diagnosing EPDS to avoid mistaking it for SCC.

Brodalumab effectively treated a man's severe hand and foot psoriasis.

Monilethrix Syndrome causes fragile, beaded hair that breaks easily and needs early diagnosis for better care.

The baby's hair loss was due to congenital syphilis, which was treated with penicillin.

Topical corticosteroids are the main treatment for Erosive Pustular Dermatosis, but recurrence is common after stopping treatment.

A patient with a thick scalp and hair loss was correctly diagnosed with alopecia areata and a thick scalp fat layer, not lipedematous alopecia, and regrew hair after treatment.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.

A 66-year-old woman's thick scalp and hair loss were confirmed as lipedematous alopecia, a rare condition possibly influenced by genetics, with no effective treatment known.

Recognizing minor skin lesions can help identify serious cancer syndromes.

Alopecia areata and lichen planus can occur together in children, which is important for diagnosis and treatment.

High-potency steroids or tacrolimus are effective treatments for Erosive Pustular Dermatosis of the Scalp.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Some leukemia treatments can cause skin reactions similar to keratosis pilaris.