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

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

Trichostasis spinulosa is a common but often unnoticed skin condition involving bundled vellus hairs, especially in people with darker skin or UV exposure.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

Overexpressing ornithine decarboxylase and v-Ha-ras in keratinocytes leads to invasiveness and malignancy.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

A painless cheek lump was misdiagnosed but later identified as a rare benign skin lesion called pilomatrixoma.

A 25-year-old man with multiple skin tumors was successfully treated with acitretin and methotrexate.

NuMA-microtubule interactions are crucial for proper skin structure and hair growth.

Steatocystoma multiplex is a skin condition starting around age 26, linked to hair follicles, and related to eruptive vellus hair cysts.

Bone marrow-derived cells contribute to skin tumors, suggesting new treatment targets for non-melanoma skin cancers.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Using special RNA to target a mutant gene fixed hair problems in mice.

Different melanocyte types in hair follicles either survive or die during the catagen phase.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

Avoiding damage and using specific shampoo and supplements improved the hair condition.

Dermoscopy is useful for diagnosing Atrichia with Papular Lesions in children without needing a biopsy.

A skin condition called pyodermatitis vegetans was found in a patient with multiple myeloma for the first time.

The analyses helped identify different skin diseases in the two dogs.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

Targeting EMT and fibrotic remodeling may help treat androgenetic alopecia.

A 30-year-old man with rare skin conditions improved with antibiotics and surgery, hinting at a link to rosacea.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

A unique gene mutation was found in a family with monilethrix.

A 15-year-old boy was correctly diagnosed with a rare skin condition after initially being misdiagnosed.

A 20-year-old woman had stable Progressive Hemifacial Atrophy and Vitiligo after treatment, suggesting a possible link between the conditions.

The study found clear differences in lesion distribution and microscopic features among trichostasis spinulosa, keratosis pilaris, and eruptive vellus hair cysts.

A specific gene mutation causes a severe skin disorder in a family.

Some hair loss disorders cause permanent loss due to scarring, and treatments like steroids don't always work well.