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Facial dark spots can be caused by the sun, genetics, makeup, or medicine, and are diagnosed by patient history and skin tests.

Lichen planopilaris in men often affects the scalp, eyebrows, arms, legs, and beard, with many having family members with hair loss.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

A 12-year-old boy's hair loss and skin issues improved significantly with medication.

Topical eyedrops may cause eyelash whitening and skin lightening around the eyes.

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

A 15-year-old boy had a rare skin growth on his buttock.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

A unique case showed a rare combination of two types of lichen planus on the face.

Hair turning darker can be a sign of skin cancer.

Dermoscopy is useful for diagnosing lichen planopilaris and certain features may relate to disease duration, age, and gender.

A 73-year-old woman with Hypopigmented Mycosis Fungoides, a rare skin lymphoma, experienced disease progression despite treatment, emphasizing the need for ongoing monitoring.

An 11-year-old girl with hair thinning was diagnosed with monilethrix and early androgenetic alopecia.

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

Lichen planopilaris mostly affects women with fair skin and can look different on each person, needing early treatment to prevent hair loss.

The study concludes that Loose Anagen Hair Syndrome is a benign condition that usually improves with age but can be hard to diagnose and stressful for the family.

A 4-year-old girl has a rare condition causing hairlessness and skin bumps, but normal teeth and sweating.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

Lichen planus commonly affects middle-aged adults, often involves limbs and mucosal areas, and can be linked to immune diseases.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

A 21-year-old male has a benign skin condition called Becker's nevus, which he chose not to treat.

Genetic factors might cause fibrosing alopecia linked to hair shaft abnormalities.

Adults can develop late-onset loose anagen syndrome, which may often be misdiagnosed.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

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.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

A 9-year-old girl has a rare hair disorder causing beaded, sparse hair.

Linear Discoid Lupus Erythematosus of the scalp can cause hair loss and should be considered in similar cases.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.