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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.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Early recognition and management of gastrointestinal tuberculosis in lupus patients are crucial to prevent complications.

Treatment with moisturizers improved the skin condition of a girl with a rare genetic skin disorder.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.

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

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

A specific gene mutation causes different hair defects in Indian monilethrix families.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A woman had temporary hair loss due to stress from a spinal cord injury.

Biotinidase deficiency can cause vision and walking problems in children and can improve with biotin treatment.

CDH3-related disease causes worsening eye and hair issues.

A man developed facial skin lesions after a stem cell transplant, which improved with specific treatments.

The study found specific skin and cell changes in patients with monkeypox, helping diagnose and understand the disease.

Merkel cell polyomavirus can infect and persist in skin cells, evading the immune system, but certain treatments can control it.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

MRI can show unusual brain changes in adrenomyeloneuropathy.

Thallium poisoning can cause worsening nerve damage and vision loss without typical symptoms.

Sexually transmitted infections and HIV should be considered as possible causes of chronic diarrhea, especially in men who have sex with men.

CD4+ lymphocytopenia can occur in patients with systemic lupus erythematosus.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

Myhre syndrome symptoms worsen over time, with specific genetic variants affecting severity.

Tick-bite alopecia can be identified by a bite-centered mark and treated with topical steroids, while SENLAT needs doxycycline.

NSC167409 can effectively inhibit the virus causing hand, foot, and mouth disease.

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

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

HIV can cause various nail and hair disorders, important for early diagnosis and treatment.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

HIV can cause unusual and severe skin problems that are hard to treat.