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A boy developed a rare skin condition after recovering from a severe skin reaction, and it improved with lotion treatment.

A specific gene mutation causes severe skin and nail issues and hair loss.

LALPS causes non-scarring hair loss along the Blaschko line, with unique trichoscopic findings.

A hand-held dermatoscope helped differentiate between pressure-induced alopecia and alopecia areata in a young patient, who then experienced hair regrowth within a month.

The dog's skin condition improved quickly with treatment and did not return.

A rare type of skin cancer on the scalp can be mistaken for hair loss, causing delayed diagnosis and severe damage.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

Eruptive vellus hair cysts are a cosmetic skin condition, more common in young adults, with few effective treatments.

Most Korean systemic lupus erythematosus patients experienced hair loss, often as non-scarring diffuse hair loss, with non-scarring patch alopecia also common.

Accurate diagnosis of Winer's dilated pore in the ear is crucial to avoid unnecessary aggressive treatment.

EPDS and MS might share an immune-related cause.

Most patients with blistering skin disorders in South India had bullous pemphigoid and often had other conditions like hypertension and diabetes.

Fibrosing alopecia in a pattern distribution is a unique hair loss condition with inflammation and scarring, resembling but distinct from common balding.

Loose Anagen Hair syndrome occurs in dark-skinned children and often improves on its own.

Early recognition and evaluation of nevus sebaceus are crucial to detect and manage potential cancerous changes.

The outer root sheath in hair follicles changes during growth, with different keratinization processes in its layers.

Fatp4 is crucial for healthy skin development and function.

Exosome therapy with laser treatment helped hair regrowth in a child with a rare skin condition.

A 17-year-old in Saudi Arabia was diagnosed with a rare skin condition causing red-brown facial patches.

Cicatricial alopecia, a permanent hair loss condition, is mainly caused by damage to specific hair follicle stem cells and abnormal immune responses, with gene regulator PPAR-y and lipid metabolism disorders playing significant roles.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

Trichoscopy helps distinguish Lichen Planopilaris from Frontal Fibrosing Alopecia by identifying unique hair loss patterns.

Dissecting cellulitis may have genetic links and can cause permanent hair loss.

Scarred skin in lichen planopilaris loses immune cells due to a decrease in a specific protein in skin cells.

Promising treatments for EBS include anti-inflammatory drugs, antibiotics, creams, mTOR inhibitors, and gene editing, but more trials are needed.

These hair loss conditions might be part of a spectrum, not separate issues.

Skin changes in Pseudoxanthoma elasticum patients can indicate the severity of related health issues.

Dermoscopic and histopathological features combined can help diagnose Pityriasis versicolor.

Dermoscopic features can help identify and differentiate types of pityriasis versicolor.