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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Pediatricians should treat some hair loss types in children and refer others to a dermatologist.

An 18-year-old girl with pemphigus vulgaris needed strong medication and careful treatment due to ineffective initial therapies and side effects.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Skin changes like hair loss, white patches, and nail changes are common in children after bone marrow transplants, often linked to chronic rejection.

The conclusion is that accurately identifying folliculosebaceous tumors requires understanding their clinical signs and microscopic features.

Tranilast successfully treated a man's skin sarcoidosis when other treatments failed.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Psychotropic medications can cause skin problems, including serious conditions, and patients should be monitored closely.

Ustekinumab might work for severe psoriasis, but more research is needed to be sure.

Children's hair loss has many causes and requires careful diagnosis and personalized treatment, including emotional support.

The document concludes that various hair and scalp disorders in children have specific treatments and proper diagnosis is essential.

Oral zinc therapy is effective for treating acrodermatitis enteropathica.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Dermatologists can help detect and manage eating disorders by recognizing skin changes.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

The dog with an Alopecia Areata-like condition showed signs of an autoimmune disease and partially regrew hair without treatment, suggesting dogs could be models for human AA research.

Hormone imbalances from endocrine diseases can cause various skin conditions that help diagnose and treat these diseases early.

A patient with total hair loss developed vitiligo after using a treatment called DCP.

Hamilton scale imprecise, hair shaft diameter decreases, stem cell transplant regrows hair, ECP ineffective for alopecia areata universalis.

Effective treatment for hidradenitis suppurativa varies, with antibiotics commonly used and surgery as an option, but no single method is universally successful.

Some skin diseases may indicate a higher risk of metabolic syndrome and related health issues.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Lichen planopilaris in men often involves scalp redness and itching, with some also having hair loss, mucosal lichen planus, or thyroid disease, and treatment improved symptoms in nearly half of the cases.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Skin problems are common in Lupus patients and can indicate the disease's severity, requiring specific treatments and lifestyle changes.

Higher antigliadin antibodies are linked to more severe alopecia areata, suggesting screening for celiac disease in these patients.

Apremilast shows promise for several skin conditions but needs more research.