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Permanent hair loss after a stem cell transplant can be a sign of chronic immune system attack on the scalp.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

Albendazole and praziquantel can cause severe side effects, especially with prolonged use or liver issues.

The role of γδT-cells in causing alopecia areata remains unclear.

A pancreatic tumor caused high glucagon levels and symptoms, but treatment reduced glucagon and shrank liver tumors.

Selenium deficiency caused symptoms in a child, which improved with selenium supplements.

Many patients with Alopecia Areata have underlying autoimmune disorders, especially thyroid issues.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Early diagnosis of colorectal cancer in young patients with certain symptoms is crucial for better outcomes.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

The hair loss in Belgian Blue crossbred calves was caused by a diet issue, not by disease or infection.

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

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Many people with inflammatory bowel disease have a vitamin C deficiency, which can lead to scurvy symptoms.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

A 7-month-old girl with a rare skin disorder died because diagnosis was delayed.

Mice with human fetal thymic tissue and stem cells developed symptoms similar to chronic graft-versus-host disease.

Feeding steers only Leucaena leucocephala causes severe health issues and poor weight gain.

Early intervention is important for limited systemic sclerosis patients due to higher pain and ulceration risks.

Brazilian patients with inflammatory bowel disease have a high rate of skin problems compared to healthy people.

Biotin supplements can effectively treat hair loss and skin issues in certain enzyme deficiencies.

Biotinidase deficiency can be easily diagnosed and treated with biotin to prevent serious harm.

A rare case linked complete hair loss to both pancreas and gallbladder cancer.

Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

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.

A leukemia patient showed skin peeling similar to kwashiorkor, a severe protein deficiency.

TGM3 is important for skin and hair structure and may help diagnose cancer.