Search

everythinglearnresearchcommunity

for

Search:↓

Some treatments for multiple sclerosis can cause hair loss.

A rare case of scleredema in a diabetic woman showed loss of sweat glands, causing heat strokes, with treatment only slightly improving symptoms.

Alopecia can be caused by multicentric reticulohistiocytosis.

A 6-year-old boy in India was diagnosed with Bloom's syndrome, showing growth and developmental issues, and skin problems worsened by sunlight.

Microbial biofilms may cause red scrotum syndrome.

Misdiagnosis of hair and scalp disorders is common in patients with skin of color, highlighting the need for better training and evaluation.

Mitochondrial dysfunction links metabolic syndrome and inflammatory skin diseases, suggesting targeted therapies and lifestyle changes.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

Patients with central centrifugal cicatricial alopecia often have higher rates of metabolic, autoimmune, and atopic conditions, as well as anxiety and depression.

People with psoriasis have more health problems, including autoimmune diseases, than those without it.

Combining medication and minimally invasive techniques can effectively manage Marine-Lenhart syndrome.

Skin diseases can cause psychological issues, and better integration of dermatology and psychiatry is needed to improve patient care.

CD19-CAR T cell therapy may help regenerate skin in systemic sclerosis.

Mutations in keratin genes cause cell fragility and various skin disorders.

Patients with mycosis fungoides have a higher risk of heart disease.

Some drugs can cause rare but potentially deadly skin reactions, and early treatment and avoiding the drug again are key.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

Non-motor symptoms in myasthenia gravis are common and need early diagnosis for better management.

Mesenchymal stem cells could help treat diabetes and its complications by improving insulin function and reducing inflammation.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

A comprehensive approach to educating patients and managing side effects is crucial for improving adherence to multiple sclerosis treatments and patient quality of life.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Managing rare genetic diseases like osteogenesis imperfecta and Escobar syndrome is complex and requires both medical and surgical treatments.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Panniculitis in dermatomyositis is rare, more common in women, and may persist despite treatment.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A strict gluten-free diet can improve liver issues in celiac disease.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

Schizophrenia patients' stem cells show abnormal neuron development and mitochondrial issues.