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Diagonal earlobe and preauricular creases may indicate higher coronary artery disease risk in men.

The Indus River dolphin has low genetic diversity due to a past bottleneck and human impact.

Non-blinded assessors tend to overestimate effects in trials by about 29%.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Caucasians have the highest hair density, followed by Hispanics, with the lowest in individuals of African descent.

A standardized scoring system is needed to improve model reliability for predicting hair loss in brain tumor patients treated with proton therapy.

Finasteride reduces prostate cancer risk by 30% without affecting Gleason scores.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

The updated GRADE guidance advises considering context when interpreting variability in research results and introduces tools for assessing subgroup effects.

The method for measuring uncertainty in finasteride tablets is reliable.

The Trichoscopy Derived Sinclair Scale offers a more accurate and reliable way to measure hair loss severity than the traditional visual method.

Certain Dibenzo derivatives may help treat prostate cancer.

Coudability hairs are useful markers for alopecia areata activity.

Dermatologists can accurately detect smaller differences in hair density than previously thought.

Doctors need to understand statistics to properly evaluate clinical trials for patient care.

Women with polycystic ovarian syndrome are more likely to have cervical insufficiency, especially South Asian and Black women.

Higher PD-1 levels are linked to fewer immune cells in hair follicles in alopecia areata.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

The new image descriptor helps identify skin cancer structures with good accuracy.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

A rigid compound with a common structural motif was successfully synthesized.

Higher power CO2 laser causes more severe skin burns and damage.

The method accurately detects diabetes with 94% effectiveness, reducing misdiagnosis risk.

Connubial contact dermatitis is often missed, making treatment harder.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.