Search

everythinglearnresearchcommunity

for

Search:↓

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Common gene patterns may cause skin autoimmune diseases.

A 61-year-old Filipino man had a skin condition that looked like another disease, making diagnosis difficult.

A 16-year-old girl with HAIR-AN syndrome was treated with lifestyle changes and medications to manage her condition.

Acne severity in women with PCOS is linked to younger age, lower body weight, and more body hair, but not to hormone levels.

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

CP-690,550 significantly reduced itching in patients with moderate-to-severe plaque psoriasis.

Fox Fordyce disease can occur in prepubertal girls and may be underdiagnosed.

Pseudopelade of Brocq is hard to diagnose and treat, with limited effective options.

A rare scalp condition with hair loss was correctly diagnosed and treated, leading to hair regrowth.

The study found unique skin changes in a rare type of alopecia linked to a skin condition called linear morphea.

Psoriasis, acne, and hair loss are linked to unhealthy cholesterol levels, increasing heart disease risk.

Autoimmune myopathy may be linked to hair loss and skin depigmentation.

Nicolaides-Baraitser syndrome may cause eczema and hair loss, needing early skin care and treatment.

PCOS affects 11% of women, highlighting the need for standardized diagnosis.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Genetic variations affecting skin structure play a key role in severe acne.

Ciclosporin can cause excessive hair growth even with testosterone blockers.

Recognizing RSCC is crucial due to its aggressive nature and high risk of poor outcomes.

Corticosteroids can reduce scarring in acne keloidalis by targeting specific cells.

Recognizing erosive pustular dermatosis of the scalp is crucial to avoid misdiagnosis.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Acitretin effectively prevented skin cancer in a patient with late-onset Rothmund-Thomson syndrome.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Psoriasis can cause hair growth in areas affected by alopecia areata.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

GLPLS is a rare skin condition with specific hair loss and skin symptoms.

Graham-Little Piccardi Lassueur Syndrome is a rare skin condition with specific hair loss and skin symptoms.

PCOS is likely inherited in families, increasing risk for first-degree relatives.

A patient with Satoyoshi syndrome improved with a treatment combining several medications, including carbamazepine and methotrexate.