Search

everythinglearnresearchcommunity

for

Search:↓

Stopping forehead irritation and using hydrocortisone helped a man's skin, Martinique has lower melanoma rates, a man had an allergy to a specific antifungal, another had unexplained cysts, certain drugs can cause skin reactions without always being interrelated, a link between Fanconi anemia and a skin condition was suggested, high levels of a certain protein may play a role in a type of psoriasis, and there's a need to study the connection between scalp pain and hair loss.

Uterine leiomyomas don't significantly change gene expression in the scalp of people with Central Centrifugal Cicatricial Alopecia.

Combining plasma rich in growth factors with hair transplant surgery may lead to faster recovery and better outcomes for hair loss treatment.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

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

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

TGM3 is important for skin and hair structure and may help diagnose cancer.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

Pregnancy can cause various skin changes and diseases, with PUPPP being the most common skin condition specific to pregnancy.

Low levels of vitamin B12 and ferritin are linked to early hair graying.

Seborrheic dermatitis may contribute to the development of central centrifugal cicatricial alopecia.

Type 2 diabetes may increase the risk of severe hair loss in African American women.

The document concludes that accurate diagnosis and treatment of scalp itch require differentiating between various conditions using a proposed five-step evaluation process.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

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

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

The document concludes that accurate diagnosis and personalized treatment are important for skin problems in women with PCOS.

No treatment has been proven to effectively stop hair loss or regrow hair in Frontal Fibrosing Alopecia, and more research is needed.

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

A genetic marker linked to a type of hair loss was found in most patients studied.

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.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

PCOS affects nearly 25% of female medical and dental students, impacting their academic and social lives.

New treatments for skin conditions related to the sebaceous gland are being developed based on current research.

Melatonin directly affects mouse hair follicles and may influence hair growth.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.