Search

everythinglearnresearchcommunity

for

Search:↓

A woman's hair loss was misdiagnosed as alopecia areata but was actually lichen planopilaris, needing immediate and ongoing treatment.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Oral JAK inhibitors are effective and safe for treating alopecia areata but may need ongoing use to keep results.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

People with Collagen VI-related myopathies may often have hair loss and scalp issues.

The document concludes that Cutaneous Lupus Erythematosus has different forms, is influenced by genetic and environmental factors, and can be treated with various medications, but more targeted therapies are needed.

Most tinea capitis patients were young boys with cat contact, had scaly patches caused by Microsporum canis, and improved with griseofulvin treatment.

The document says homoeopathic treatments are good for hair regrowth in alopecia areata but doesn't give proof.

EGFR inhibitors often cause skin problems and other side effects, but these are usually reversible and can be managed to keep patients comfortable.

Traditional knowledge of edible oil-producing plants in Sinja Valley is declining due to outmigration and sociocultural changes.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Minoxidil can help transgender males grow facial hair before starting testosterone therapy.

Shift nurses show altered body temperature and stress hormone levels, suggesting their body clocks adjust to irregular schedules.

The document concludes that while there are various treatments for Alopecia Areata, there is no cure, and individualized treatment plans are essential due to varying effectiveness.

The document concludes that surgery is a preferred treatment for cicatricial alopecia, with the method chosen based on individual factors and may require multiple sessions and careful postoperative care.

Shrinking skin cancer increases the chance of cancer in nearby lymph nodes.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Acne can be managed with various treatments and requires psychological support due to its emotional impact.

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.

A boy's hair loss improved after tumor removal and vitamin D treatment, but hair loss returned despite normal vitamin D and no tumor regrowth.

There may be a connection between Frontal Fibrosing Alopecia and Lichen Planus Pigmentosus, and more research is needed to confirm this.

Many skin patients also have mental health issues, and doctors should treat both together.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

The article concludes that cranial reconstruction should aim for the best aesthetic result, using various techniques tailored to individual needs and conditions.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Mesotherapy shows promise for cellulite and facial rejuvenation but has mixed results for body sculpting and hair loss, with more research needed for safety and effectiveness.

Scalp cooling can reduce chemotherapy-induced hair loss and should be available in all hospitals.

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

Early treatment of children's hair loss, which can be caused by various factors, is important due to its emotional impact.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.