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Genetics and nutritional deficiencies are key factors in premature graying of hair.

Female pattern hair loss has multiple causes and treatments, with new therapies showing promise.

Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Most hospitalized children with skin issues were boys, with allergic skin diseases like atopic dermatitis being most common, and treatments were usually topical.

Alopecia areata is caused by immune system issues, and JAK inhibitors might help treat it.

Changing CDK4 levels affects the number of stem cells in mouse hair follicles.

The summit concluded that new treatments like Jak inhibitors show promise for Alopecia Areata and personalized approaches are needed.

Alopecia areata and vitiligo share immune system dysfunction but differ in specific immune responses and affected areas.

Androgenetic alopecia is a common hair loss condition influenced by various factors and linked to psychosocial and cardiovascular issues.

Different types of female pattern hair loss have unique characteristics and are associated with various health conditions.

Certain immune molecules and stress affect hair loss, and while genes play a role, more research is needed to fully understand and treat it.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

Genes linked to wool fineness in sheep have been identified.

More young women are getting diagnosed with PCOS, which can lead to other health problems, but early treatment can help.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

Hirsutism, excessive hair growth in women, often caused by high androgen levels and polycystic ovary syndrome, can be treated with medication and weight management.

A postmenopausal woman with hair loss and hirsutism improved after surgery to remove an ovarian tumor.

Primary cicatricial alopecia, a rare disorder causing permanent hair loss, is hard to diagnose and treat, with treatments like anti-inflammatory drugs and steroids offering varied results and no guaranteed cure. Psychological support for patients is important, and future research should aim to identify causes of the condition.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

A child with a rare vitamin D-resistant condition improved with treatment.

Human skin xenografting could improve our understanding of skin development, renewal, and healing.

Premature aging increases the risk of immune problems and autoimmune diseases.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.