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The patient with lupus and Degos' disease showed significant improvement with treatment.

Two siblings were diagnosed with Trichothiodystrophy, identified by brittle hair and low sulfur content.

The model improves understanding of androgen interactions by focusing on signal intensity and system capacity.

A rare case of isolated trichothiodystrophy was identified, marked by brittle hair with low sulfur content.

TSPO might help treat anxiety and depression.

Chitosan glycolate and lactate sponges are promising for wound healing, while chitosan ascorbate sponges are less effective.

A specific gene mutation causes Olmsted syndrome.

Combination therapy with oral contraceptives and spironolactone improves hair growth, menstrual issues, and acne in women with PCOS.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Sorafenib may cause hand-foot and stump syndrome, requiring early detection and management.

Sensitive scalp has higher pH, more redness, abnormal sebum, and altered bacterial makeup.

Trichostasis spinulosa can look like acne but usually affects adults, not children.

Biotin, alone or with minoxidil, effectively treats short anagen syndrome.

Systemic sclerosis skin shows varied gene patterns, suggesting potential for personalized treatment.

DKK2 and SOSTDC1 together are necessary for the normal timing of the first regression phase in the hair growth cycle.

Sickle cell disease affects BMI and pain frequency, with HbSS patients having more pain and unhealthy BMI.

AQB reduces harmful skin changes in systemic sclerosis.

The EFSUMB created basic guidelines for using ultrasound in skin-related medical practice.

Prinsepia utilis seed oil is suitable for making pharmaceutical soap.

Spironolactone helps reduce fluid in the eye in Central Serous Chorioretinopathy, but doesn't improve vision and recurrence is common.

Targeting SIRT1 with antisense oligonucleotides could be a promising treatment for hair loss.

Removing SIX1 in fat cells reduces skin fibrosis.

Facial trichostasis spinulosa is a chronic condition with significant cosmetic impact, especially in young women.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.