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BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

The young goat had anaplasmosis and copper deficiency.

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

Vitamin B12 deficiency can cause reversible skin darkening.

Upadacitinib can cause hypersensitivity that worsens ulcerative colitis symptoms.

The hair disorder was caused by abnormal protein formation, making hair easily damaged.

Catatonia can be a rare sign of lupus, needing careful diagnosis and treatment.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

A 16-year-old boy had pernicious anemia, autoimmune hemolytic anemia, and later developed alopecia areata.

ILC1-like cells can cause alopecia areata by disrupting hair follicle immunity, suggesting a new treatment approach.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Excessive selenium intake can cause liver damage.

A woman's hair loss and skin discoloration were found to be caused by a rare case of leprosy on the scalp, not alopecia-vitiligo overlap.

Vitamin B12 deficiency can cause reversible hair color loss in children.

People with mycosis fungoides/Sézary syndrome have a much lower quality of life.

Early and accurate diagnosis of primary vitreoretinal lymphoma is crucial to prevent serious complications.

Cytotoxic T cells cause hair loss in chronic alopecia areata.

Lugol's solution can cause thyroid problems if used long-term for non-approved reasons.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

The dog's skin and anemia issues returned after stopping treatment for Babesia gibsoni.

Giant cells found in some male pattern baldness cases may help diagnose it and suggest hair is mistakenly seen as foreign by the body.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

The man's rash, hair loss, and vision issues were due to syphilis, not CMV.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

Pegylated interferon-alpha 2a can cause a rare nerve disorder, but early treatment can lead to full recovery.

IV cyclophosphamide effectively treated severe lupus nephritis in Indian patients.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.