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LC-OCT can help identify lupus-related scarring hair loss by spotting unique features.

Epidermolysis bullosa in calves was not caused by mutations in the keratin genes bKRT5 and bKRT14.

Argentine-cross polo ponies commonly develop sarcoid tumors with distinct types and histopathological features.

Lichen planus pigmentosus causes dark skin patches and is treated by avoiding triggers and using anti-inflammatory medications.

A young child with alopecia areata and psoriasis improved with treatment, suggesting a link between the two conditions.

Deleting vitamin D and calcium receptors in skin cells increases skin cancer risk by reducing DNA repair and stress response.

Pigmented rings with central clearing help diagnose melasma more accurately.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

Trichoscopy can reveal specific hair and scalp changes in linear morphea.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

Transplant patients often get skin problems, with treatments varying by condition.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Chemotherapy improved a girl's painful foot condition linked to pachyonychia congenita.

Two patients with lupus had an unusual type of hair loss not typical for the disease.

Elderly patients with eruptive skin bumps may have clear cell syringoma linked to glucose issues.

Hair loss in systemic lupus erythematosus patients is unique and improves with treatment.

Netherton syndrome is a genetic skin disorder causing severe skin issues and requires careful treatment to protect the skin barrier.

Skin cancer in sun-exposed areas is more likely to come back.

IL10_ApoEVs improve skin healing and reduce scarring.

Erosive pustular dermatosis is a rare skin disease that's hard to treat and affects the scalp or legs.

Umbilical cord blood transplantation improved the boy's symptoms despite complications.

Melasma is a skin condition linked to female hormones, genetics, UV exposure, and certain medications, but not to pituitary, adrenal, or thyroid diseases.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

The circadian clock is crucial for tissue renewal and regeneration, affecting stem cell functions and having implications for health and disease.

Ginseng and its compounds may help hair growth and prevent hair loss, but more human trials are needed to confirm this.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

Laser treatment improved scalp skin condition with no side effects.