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Psoriasis patients did not show more brain atrophy or small vessel disease than controls, but longer psoriasis duration was linked to more brain atrophy.

Sca-1+ cells in newborn mouse skin may become fat cells.

A rare ear-area hair cyst was successfully removed from a 10-year-old boy.

Three Iranian men had reddish-brown facial pigmentation with no effective treatment.

Lack of small, fine hair on the front hairline is a key sign of frontal fibrosing alopecia.

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

Fibroblasts from healthy donors can prevent changes seen in recessive epidermolysis bullosa simplex.

Lizard claws have hair-like keratins similar to those in mammals.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Wet cupping blood has different components than regular venous blood, which might affect skin disorder treatments.

A painless cheek lump was misdiagnosed but found to be a rare, benign skin lesion called pilomatrixoma, treatable by surgery.

The study found a unique vein pattern around the aorta and two arteries in the right kidney.

Cubosomes improve drug delivery for skin and eye diseases by enhancing adhesion, retention, and release.

Enlarged facial pores are denser, more contrasted, and linked to changes in skin structure and hair follicles.

Krox20 overexpression in fibroblasts may play a role in abnormal scar formation and could be a target for new treatments.

A rare case of Cushing's syndrome and pheochromocytoma requires careful re-evaluation to avoid complications.

Pathologic tissues have more soluble proteins than normal tissues.

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

An unusual growth of Leydig cells in a woman's ovaries caused her excessive hair growth, which was treated successfully with surgery.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

Diagnosing Sertoli-Leydig cell tumors is challenging due to their unusual symptoms and can occur at any age.

The ventral matrix is the main source of the nail plate.

Recognizing rare tumor combinations is crucial for accurate diagnosis and treatment.

A specific gene mutation causes Olmsted syndrome.

Horizontal sections of scalp biopsies are good for diagnosing Central Centrifugal Cicatricial Alopecia and help customize treatment.

Detecting early breast arterial calcifications can help assess cardiovascular disease risk.

Blood vessels and specific genes help turn cartilage into bone when bones heal.

CCCA is a common, progressive hair loss condition that may not always be linked to hair care practices and requires a biopsy for diagnosis.