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Looking at tissue characteristics isn't reliable for telling apart basal cell carcinoma from certain benign skin tumors.

The number of new cases of cutaneous B-cell lymphoma has leveled off since the early 2000s, and survival rates have improved since 1973.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Narrowband-UVB phototherapy successfully treated a rare case of Graham Little-Piccardi-Lassueur syndrome.

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BBS7 is essential for healthy gums by supporting cell function and blood flow.

The U.K. created the CPSA to set safety standards for non-surgical cosmetic treatments and improve patient protection.

CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

The new method is rapid, sensitive, and accurate for evaluating the quality of the medicinal herb Platycladi cacumen.

Complex basal cell carcinomas need personalized treatment due to unique genetic mutations.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

Early detection and biotin treatment improve outcomes for biotinidase deficiency.

Basonuclin helps identify and track hair follicle development and cycling in mice.

Researchers created a new system to classify male baldness, finding six types and a common hairline shape, to improve hair loss treatments.

KLHL24-mutant stem cells help understand skin and heart disease.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Dr. Russell Knudsen's system classifies hair grafts by class, shape, and size for clearer communication in hair restoration surgery.

Bexxar treatment led to a high response rate in patients with advanced-stage, treatment-resistant follicular lymphoma.

The Facial Psoriasis Log-based Area and Severity Index is a more effective way to measure improvements in facial psoriasis than the traditional method.

Homeopathy improved hair health and emotional well-being in severe female baldness.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Experts recommend starting systemic treatment for alopecia areata when the condition is severe or causes significant distress.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

Horse skin diseases are complex to manage and often require a biopsy for accurate diagnosis and treatment.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.