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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

An 87-year-old woman was diagnosed with type 3 autoimmune polyendocrine syndrome and had multiple autoimmune issues.

Brodalumab effectively treated a man's severe hand and foot psoriasis.

Hair loss in three Southeast Asian women with kidney failure may be linked to their anemia treatment with erythropoietin.

Rituximab effectively treated a woman's bone lymphoma that was resistant to other treatments.

Netherton syndrome in a boy caused skin and hair issues, and treatment didn't work.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

A 6-year-old girl had both monilethrix and trichorrhexis nodosa, causing brittle hair, with minimal improvement from treatment.

ALRN-6924 can protect hair follicles from chemotherapy damage by temporarily stopping cell division.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

The patient had paraneoplastic pemphigus without mucosal involvement.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Anti-PD-L1 immunotherapy can cause hair loss and unexpected hair color change, but treatment can restore hair growth and color.

A child's rare skin disease was triggered by chickenpox.

Alopecia areata can be transferred through stem cell transplants from affected siblings.

Oncology specialists are disappointed by the discontinuation of the effective lymphoma treatment Bexxar.

Skin pigmentation increases in CRPS-affected areas and improves with symptom relief.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

A rare EGFR mutation in newborns leads to severe health issues and early death.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

The combination of mitoxantrone, etoposide, and prednisolone is effective for treating relapsed lymphoma with manageable side effects.

Minoxidil can cause temporary vision loss and color blindness.

The newborn's skin condition improved over time, leaving only lighter skin patches.