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A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

Organoid technology is advancing and entering commercial use, with applications in disease modeling, drug development, and personalized medicine.

Vδ1+ T-cells in the skin contribute to hair loss in alopecia areata and could be targeted for treatment.

An 80-year-old woman with Cronkhite-Canada syndrome had multiple polyps and symptoms like diarrhea, hair loss, nail issues, and dark skin.

Miliacin helps damaged hair follicles grow new hair faster.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

The man has a genetic skin condition called pachyonychia congenita.

A baby with KID syndrome died from infections and organ failure at 18 months old.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

New drugs for Alzheimer's and rheumatoid arthritis advanced, a Zika vaccine is in development, and there were business deals in anesthesia and oncology.

An 8-year-old girl had nail and hair issues that improved without specific treatment, but fungal nail infection was hard to cure.

Japanese researchers created new hair follicles from human cells that grew hair when put into mice, and other findings showed a link between eye disease severity and corneal thickness, gene mutations affecting hearing and touch, and the safety of the shingles vaccine for adults over 50.

In 2002, various skin reactions were reported due to different drugs, including allergies, hair loss, skin lesions, and other skin conditions.

Prostaglandin helps regenerate hair follicles after radiation damage.

The author clarified that Alopecia Areata Incognita (AAI) and diffuse Alopecia Areata (AA) are different conditions and the case discussed was actually AA, not AAI.

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.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Chemotherapy can cause various skin problems, and recognizing them helps improve patient care.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

A patient with Cronkhite-Canada syndrome improved with nutritional support and steroids, but early diagnosis is key due to high mortality.

Baricitinib may effectively treat nail changes in alopecia areata.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Adults with Beta Thalassemia Major are more likely to have skin, hair, and nail disorders.

Prednisolone improved symptoms in a woman with Cronkhite-Canada syndrome, but regular screenings are needed due to cancer risk.

Alopecia areata may appear differently depending on the individual's type of hair loss and scalp condition.