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Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

Shock can be an early sign of Autoimmune Polyendocrine Syndrome Type II.

The boy's genetic diagnosis of ectodermal dysplasia helped improve management and counseling for him and his sister.

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

Certain genes are linked to the risk of developing Alopecia Areata.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Reduced Stx17 expression may contribute to Alopecia Areata.

Three molecular subtypes of advanced skin T-cell lymphoma were identified, with potential biomarkers for predicting treatment response and disease progression.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Researchers found a new mutation causing total hair loss from birth.

Stress can cause sudden hair whitening in children, but it may reverse on its own.

Vogt-Koyanagi-Harada disease affects vision and skin, mainly in people with darker skin, and is treated with steroids and immunosuppressants.

Stress can cause sudden hair whitening in children, but it may reverse on its own.

Wearing a wig caused a woman's skin condition to worsen due to pressure from the wig's fasteners.

The woman's hair loss might be due to a chronic infection.

Down Syndrome patients with Alopecia Areata often have hypothyroidism and specific immune abnormalities.

A unique hair tumor with a rippled pattern was identified, showing incomplete differentiation and unusual cell arrangements.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

Wearing a wig caused a skin condition to develop in a woman with hair loss.

The document concludes that a woman has both Frontal Fibrosing Alopecia and Lichen Simplex Chronicus, a previously unreported combination of conditions.

Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

Brunsting-Perry pemphigoid can cause scarring hair loss and may be underdiagnosed.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

The document concludes that anticonvulsants like phenytoin may cause skin reactions by affecting tryptophan metabolism and suggests researching vitamin levels in patients with drug reactions.

Reduced matriptase activity causes skin and hair issues in both humans and mice.

A new gene mutation causes insulin resistance in a girl and her mother.