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Lichen simplex chronicus on the scalp can be diagnosed by specific hair and skin signs and treated with corticosteroids and therapy.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Rathke’s cleft cysts can rarely cause Cushing disease, and surgery can improve symptoms.

Tinea capitis should be considered for scalp infections in infants.

Three skull models were found most useful for testing hydrocephalus valve programming.

Trichostasis spinulosa is a rare skin condition with hair-filled plugs in hair follicles.

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

Early physiotherapy with exercises and stretching is crucial for treating congenital torticollis.

The man likely has secondary syphilis affecting his nervous system.

Vibration assisted analgesia reduces pain during corticosteroid therapy for alopecia.

Early biotin treatment can reverse symptoms of congenital biotinidase deficiency.

A woman's male-like symptoms and high testosterone were due to ovarian hilus-cell hyperplasia, which improved after surgery.

Surgical removal of abnormal fat pads fixed the woman's eyelid issue caused by likely silicone injections.

Surgical excision is the best treatment for SCC, but intralesional cidofovir might be a viable alternative.

Early diagnosis of PSIS can lead to normal height with growth hormone and testosterone treatment.

Biotin treatment improves symptoms of biotinidase deficiency, but some neurological damage may be permanent.

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

Trichostasis spinulosa is a common but often unnoticed skin condition involving bundled vellus hairs, especially in people with darker skin or UV exposure.

A young woman's rare ovarian tumor was successfully removed, improving her hormonal symptoms.

A 79-year-old man was diagnosed with a rare skin condition called nevus comedonicus on his eyelids.

Some families have a genetic condition where they are born with irregular scalp defects.

Selumetinib significantly reduced tumor size and improved vision in a child with neurofibromatosis type 1.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

Adrenomyeloneuropathy (AMN) can cause bladder problems due to nerve damage.

Decreased IGF-1R expression may contribute to sacrococcygeal pilonidal sinus development.

The study found clear differences in lesion distribution and microscopic features among trichostasis spinulosa, keratosis pilaris, and eruptive vellus hair cysts.

Researchers identified a new hair loss pattern called "sisaipho type," where hair is lost across the scalp except around the edges.

Ethosomes can safely and effectively deliver various drugs deep into the skin.