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Herpes gestationis is linked to certain antigens, atopic eczema affects T cell populations and may be eased by breastfeeding, higher doses of anti-androgen treatment can improve androgenic alopecia, topical minoxidil increases hair thickness, long-term methotrexate therapy can cause liver fibrosis in psoriasis patients, and Lichen Sclerosus et Atrophicus patients aren't at higher risk for autoimmune disorders.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

Skin symptoms are important for diagnosing infections in children.

The meeting discussed various skin conditions, treatments, and unusual cases, highlighting the effectiveness of tetracycline in treating rosacea.

Dermatological conditions are complex and treatments often have mixed results.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

TTD hair brittleness is caused by multiple structural abnormalities.

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

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

The document suggests a new way to categorize skin and mind disorders into two main groups to reduce confusion.

Alopecia Areata is linked to a higher risk of several diseases, which vary with age and sex.

Epidermolysis bullosa is a genetic disease causing fragile skin and blisters in both animals and humans.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

A 46-year-old man showed symptoms of a rare condition usually seen in postmenopausal women, highlighting the need for dentist-dermatologist collaboration.

Hair regrowth was seen in 83% of children with alopecia, immune system plays a role in the condition, and various treatments showed effectiveness for hair and nail disorders.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

HIV can cause unusual and severe skin problems that are hard to treat.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

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

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

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

SJS/TEN survivors often have severe, overlooked long-term physical problems that are not properly treated after leaving the hospital.

Alopecia Areata is an autoimmune disease affecting hair follicles, influenced by genetic and environmental factors, with rodent models being essential for research.

Women experience various skin issues at different life stages, requiring careful treatment and awareness.

The document explains the genetic causes and characteristics of inherited hair disorders.

Mutations in the KRT85 gene cause hair and nail problems.