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Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Systemic corticosteroids can cause unusual skin issues in people with juvenile rheumatoid arthritis.

Accurate diagnosis of SLE requires extensive testing due to its complex symptoms.

Skin problems are common in kidney disease, with dry skin and itching in patients not on dialysis or on hemodialysis, and infections most common in transplant recipients.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Sports influence skin condition names and help in diagnosis and treatment.

Cell-mediated drug delivery systems improve skin disease treatment by using living cells for precise, prolonged, and less toxic therapy.

Skin changes can signal diabetes and metabolic issues, aiding early diagnosis and treatment.

Almost all patients with chronic kidney disease not yet on dialysis have at least one skin problem.

Celiac disease can cause skin issues, and a gluten-free diet can help improve them.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Alopecia areata may increase the risk of cardiovascular disease.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Doctors should consider comedonic discoid lupus erythematosus to avoid misdiagnosis.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Some children with COVID-19 develop skin symptoms linked to a severe inflammatory condition.

Endocrine disorders can cause various skin and hair issues.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Skin symptoms like rashes and hives can help identify COVID-19 early.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

A woman had a rare skin condition with recurring painful nodules that heal in 6 weeks, often without needing treatment.

Effective treatment improved skin and overall symptoms in a lupus patient.

The man's diarrhea was caused by a rare disorder called Cronkhite-Canada syndrome, which improved with specific medications.

Cronkhite-Canada syndrome causes chronic diarrhea and has a poor prognosis despite treatment.

Certain skin conditions in women are linked to higher risks of metabolic syndrome and type 2 diabetes due to hormone imbalances.

Two cases showed skin abnormalities without bone or neural defects.

Mutant keratins cause inflammation in Epidermolysis Bullosa Simplex, suggesting targeting them could help treat the disorder.

Alopecia, especially androgenic, may increase cardiovascular risk, but more research is needed.