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DHT deficiency may disrupt rat epididymis function by affecting estrogen receptors.

Dkk4 is necessary for the initial development and arrangement of hair follicles.

Dermoscopy can help diagnose tuberous sclerosis by identifying unique skin patterns.

Foals with Rhodococcus equi infection often have other health problems that lower their chances of survival.

A girl grew extra hair in areas where she had insect bites.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

Eph receptors and ephrins may be promising targets for treating diseases, but more understanding is needed for effective and safe therapies.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

A man with a rare lung-focused form of hypereosinophilic syndrome improved with steroid treatment.

Dkk4 protein is necessary for the proper development and arrangement of hair follicles.

Feather pigment patterns form through melanocyte arrangement and simple regulatory mechanisms.

The junction of the inner and outer prepuce with good blood flow is best for vascular pedicle flaps.

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

Prostaglandin E2 affects human platelet activity in complex ways that could lead to personalized heart disease treatments.

A baby with KID syndrome died from infections and organ failure at 18 months old.

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

Vertex accentuation is a common pattern in female hair loss.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

A new type of nerve cell involved in itch perception was discovered.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

A rare hair regrowth pattern can occur in some people with alopecia areata.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.