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CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

Normal cells outcompete and remove mutant cells in the pancreas with the help of the EphA2 receptor.

Radiation cystitis patients need better monitoring and early treatment due to higher readmission rates.

Forehead taping can sometimes lead to unexpected problems.

A man with itchy skin lesions and weight loss was diagnosed with a rare skin condition linked to a pancreatic tumor.

A 65-year-old man with sudden abdominal pain and seizures was diagnosed with a rare, non-traumatic splenic rupture and treated without surgery.

Hair transplantation can lead to rare scalp complications, requiring careful follow-up and treatment.

Botulinum toxin A effectively treated a man's facial cysts with no side effects and lasting results.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

Tiny infundibular cysts are the main lesions in chloracne, not comedones.

Fungal infections should be considered in scalp swelling to avoid misdiagnosis.

Three genes linked to the development of trichilemmal cysts were found.

A 21-year-old male has a rare scalp condition with excessive skin folds.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

A woman had a unique skin growth with hair follicle, oil glands, fat cells, spindle cells, and nerve fibers.

A man developed a rash similar to pityriasis rubra pilaris after starting sorafenib for cancer, possibly due to the drug's effect on skin cells.

A 4-year-old girl has a rare condition causing hairlessness and skin bumps, but normal teeth and sweating.

A patient with Rhupus was diagnosed with Rowell syndrome and treated with various medications.

A 6-year-old girl with head lice developed scarring hair loss but improved with treatment.

Steatocystomas are harmless skin cysts that can vary in size and may sometimes cause itching or pain.

Kerion is a severe scalp infection that needs quick treatment to avoid permanent hair loss in children.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

A man with scalp and neck skin issues improved after a year of oral isotretinoin.

A 21-year-old had a rare developmental anomaly with a misplaced sebaceous gland in a hair follicle.

GRK2 is essential for healthy hair follicle function, and its absence can lead to hair loss and cysts.

The triple rotation scalp flap technique successfully reconstructed a man's scalp with natural-looking hair growth and minimal scarring.

A 10-year-old boy was diagnosed with a rare scalp condition causing hair loss and treated with a topical cream.

Double trichophytic closure effectively repairs thin scalp scars, reducing financial burden.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.