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"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

Androgen receptors are active in many tissues of both male and female mice, not just reproductive organs.

Longer anogenital distance may indicate a higher chance of having polycystic ovary syndrome, and measuring this distance along with hormone levels could improve diagnosis.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Redefining disfigurement could improve the current law's effectiveness.

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

Androgens increase muscle mass by promoting myoblast growth through ornithine decarboxylase.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

DACC-based dressings are more effective than silver-based ones for treating chronic wounds with antimicrobial resistance.

Dark hair with a red beard likely evolved for camouflage, not attraction.

5α-reductase enzymes are crucial in certain disorders, and while treatment advances exist, more research on SRD5A3 is needed.

A specific gene mutation causes a severe skin disorder in a family.

Certain immune cells in atopic dermatitis skin could be targeted for treatment.

Upadacitinib effectively treats severe alopecia areata and is safe.

Trace element deficiencies may contribute to diffuse alopecia.

Certain skin proteins can form anchoring structures without the protein AMACO.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

RCM and dermoscopy help identify different types of hair loss in children.

New oral anticoagulants are safer and easier to use with new reversal agents for bleeding emergencies.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Acanthosis nigricans is common in obese individuals, but not significantly linked to obesity type.

PRAME helps distinguish between benign and malignant skin cells in most cases.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

A reliable method was developed to measure aristolochic acid-I in rat blood.

Dermatologists are key in detecting and managing OCD and BFRBs by working with psychiatrists.

Monoclonal antibodies are often linked to alopecia areata cases.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Baricitinib improved severe hair loss in adults over 52 weeks and was safe to use.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

Balding people may have higher heart disease risk.