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Patients with central centrifugal cicatricial alopecia may have a higher risk of breast and colorectal cancer.

Acne keloidalis nuchae is a tough-to-treat condition that greatly affects quality of life, especially in men of African descent.

Aggressive immunosuppressive treatment improved a woman's severe heart condition linked to autoimmune disease.

A woman with rheumatoid arthritis had a unique type of scarring hair loss not caused by infection, requiring early treatment to avoid permanent hair loss.

A 15-year-old boy's severe scalp condition improved significantly with adalimumab and baricitinib treatment.

A young woman had a rare skin reaction to a medication for her joint disease, and a combination therapy improved her condition.

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

A single steroid injection can cause serious side effects like Cushing Syndrome.

Acitretin helped improve hand mobility and skin condition in a patient.

Isotretinoin treatment improved scalp condition and stopped hair loss.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

An 80-year-old man with COVID-19 also had constrictive pericarditis, possibly due to an autoimmune or immunoglobulin related disease, and improved after surgery.

A newborn girl has a rare skin condition with two ulcers on her buttock that are healing on their own.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

The combination therapy effectively improved acne keloidalis nuchae.

Congenital atrichia with papular lesions causes permanent hair loss in children.

A rare cataract surgery complication was successfully treated with laser capsulotomy.

Early diagnosis and multidisciplinary care, including orthopedic surgery, can prevent long-term disability in IFAP syndrome.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

Knuckle Acanthosis Nigricans is common in Latin American youth and may indicate early insulin resistance, especially in those with normal weight.

The family has a unique form of ectodermal dysplasia similar to Clouston syndrome but with different hair and skin symptoms.

CCL 27 levels are similar in people with and without alopecia areata.

Giant keratoacanthoma can look like squamous cell carcinoma, requiring careful diagnosis and surgical removal.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Recurrent pneumothorax can occur in Sjogren's syndrome, even without common markers.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

Janus kinase inhibitors may effectively treat resistant scalp conditions like folliculitis decalvans and dissecting cellulitis.