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Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Clouston syndrome can lead to skin cancer, so monitoring is crucial.

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

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

Always consider xanthomatous hypophysitis before deciding on pituitary surgery.

Surgery on a baby with a skin disorder improved eyelid position and eye health.

Strontium ranelate helps cartilage growth by blocking a specific cell pathway.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

Trichoscopy helps diagnose and monitor the treatment of fungal scalp infections in children.

The letter argues that blaming synthetic hair implants for scalp cancer based on one report is biased and possibly coincidental.

A rare ovarian tumor was diagnosed in a woman from North Brazil, and surgery is the preferred treatment.

More than half of patients who had acromegaly surgery experienced hair loss, with varying degrees of recovery.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Trichilemmal cysts may form from hair follicle outer root sheath growth.

A child with a rare scalp condition regrew hair after treatment.

The snail flap technique is an easy, reliable, and hair-preserving method for scalp reconstruction, especially good for elderly or frail patients.

Scalp sarcoidosis can cause hair loss and needs accurate diagnosis and treatment with specific medications.

A woman was diagnosed with Sheehan's syndrome and a rare complication of diabetes insipidus 33 years after symptoms began, improving with hormone therapy.

A unique type of complex cyst was found on a man's scrotum.

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

Mutations in the HOXC13 gene cause hair and nail development issues.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Ketoconazole effectively treated a scalp infection in a 6-year-old boy, leading to full recovery.

Renal transplant patients on tacrolimus and sirolimus may develop acne keloidalis nuchae.