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The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Vascular patterns in dermoscopy help tell apart malignant and benign skin tumors.

A possible link exists between hair follicle abnormalities, hair loss, and muscle weakness.

The newborn's skin blisters healed without scarring, leaving some light spots, and stopped forming after four months.

Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

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

Lymph vessels in airways vary by location, with the most in the upper pharynx and changes after birth.

A woman with cervical cancer had rare scalp metastasis causing a unique type of hair loss.

Breast cancer skin metastases are rare, look different, and can be confused with other skin issues, so a biopsy is needed for accurate diagnosis.

A man's scalp condition was misidentified as hair loss dots but was actually a common follicular disorder.

A rare scalp condition causing hair loss and cysts in young men can be treated effectively with a specific steroid injection.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

Different sebaceous gland diseases can be treated with medications, hormone therapy, or surgical methods.

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

Topical rapamycin may effectively treat fibrous papules on the face.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

BerEP4 and CD34 staining can help tell apart tricholemmoma from basal cell carcinoma.

A man with follicular psoriasis got better after treatment with skin cream and allergy pills.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

LC-OCT helps accurately diagnose different types of infant hair loss without invasive methods.

Fibroblasts can be mistaken for neural cells, so functional validation is needed.

Thymic LCH may be underdiagnosed, so thymic ultrasound should be considered in infants with cutaneous LCH.

Neprilysin is important for hair growth regulation.

Different growth patterns in thyroid tumors are influenced by where cell growth and death occur.

Nestin-expressing cells turn into a specific type of skin cell in hair follicles during development and in adults.

A cancer drug called nilotinib might cause hair loss due to inflammation around hair follicles.

Pigmented rings with central clearing help diagnose melasma more accurately.