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Early treatment of EPDS can improve outcomes and reduce recurrence risk.

Scalp involvement is common in pemphigus and can lead to hair loss, with the severity of scalp lesions linked to overall disease severity.

A man's skin condition, pemphigus vulgaris, came back after he was treated with interleukin 2 for cancer.

Hair straightening treatments can cause serious kidney damage, especially if you have skin issues.

Strong skin creams work well for long-term scalp inflammation in Rapp-Hodgkin Ectodermal Dysplasia.

Scalp involvement in pemphigus means the disease is more severe and harder to treat.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Hair loss is a rare but recognized symptom of pemphigus vulgaris, with patients usually regrowing hair after treatment.

The conclusion is that using the 5W1H method can improve diagnosis and management of childhood hair-pulling disorder.

The link between pemphigus and the patient's scarring hair loss is still unclear.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

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.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Early and aggressive treatment is crucial for preserving vision in infants with AEC syndrome.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

The conclusion is that high-potency steroids or tacrolimus are effective treatments for erosive pustular dermatosis of the scalp.

Hair loss in autoimmune blistering skin diseases varies and may regrow with disease control.

Breast cancer skin metastases are rare, look different, and can be confused with other skin issues, so a biopsy is needed for accurate diagnosis.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.