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Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

The tumor on the man's nose was a rare type called pedunculated follicular hamartoma.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Mogamulizumab can cause hair loss and skin rashes.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

Recognizing unusual symptoms in Crohn's disease is crucial for proper treatment.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

It's important to consider genetic hair disorders when diagnosing hair loss.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Melanocytic matricoma can look like skin cancer but is usually harmless; surgery and follow-up are advised.

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

A woman with non-classic CAH had unusual heavy periods and high hormone levels, improved with treatment.

A boy with GAPO syndrome had hair loss similar to male pattern baldness without hormone issues, possibly due to skin or blood vessel problems.

Three Iranian men had reddish-brown facial pigmentation with no effective treatment.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A man with a birthmark on his scalp developed hair loss that improved with treatment, but the link between the birthmark and hair loss was unclear.

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

A 33-year-old woman with PCOS and metabolic syndrome was unusually diagnosed with a bone condition called DISH, suggesting a possible link between these conditions.

A woman's skin symptoms led to a diagnosis of systemic AL amyloidosis, but she died from sepsis shortly after.

The scalp has a natural speckled pattern of increased pigment around hair follicles, possibly linked to local hormone production.

A woman's shingles infection triggered her first episode of a rare neurological disorder and blood vessel inflammation.

A woman's male-pattern facial hair growth was caused by a rare malignant ovarian tumor that was difficult to diagnose and treat.

An 87-year-old man showed unusual signs of Hodgkin lymphoma, primarily high calcium levels, which improved after treatment and revealed the disease.

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

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.