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Thymoma may link myasthenia gravis, nail dystrophy, and alopecia areata.

Graham-Little syndrome causes scarring hair loss and skin bumps.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

A large scalp tumor was removed from an elderly woman, who was later diagnosed with schizophrenia.

The study found that hair transplant surgery can be used to treat a rare condition that causes a band of hair loss, but surgeons should check for skull abnormalities first.

A rare gene variant causes hair and nail issues in a family.

Patients with RASopathies have a higher risk of autoimmune disorders and should be routinely screened.

The man has a genetic skin condition called pachyonychia congenita.

New mutations in the hairless gene may cause hair loss and affect bone development.

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

Systemic mastocytosis may cause a type of hair loss called cicatricial alopecia.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

Cantú syndrome may be linked to pituitary adenomas.

Removing the liver tumor improved the patient's skin condition and hair growth.

Netherton Syndrome can cause severe skin lesions in rare cases.

A young girl's foot lesion was actually a rare condition caused by a hair fragment under the skin, not a parasite.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

A woman experienced unusual hair loss and skin reactions after taking phenobarbital, but her hair grew back after treatment.

Genetic hair shaft abnormalities can be seen with microscopes and often affect scalp hair.

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.

Looser dietary restrictions can improve growth and reduce illness in methylmalonic acidemia patients.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

A new gene mutation linked to a skin condition was found in a Spanish family.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The case suggests a possible link between severe acne and certain bone deformities.

Keratin 14 may be an autoantigen in autoimmune skin diseases.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Netherton's syndrome can cause frequent bacterial infections beyond just skin issues.