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Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

The patient's long-term hair loss was caused by leukemia treatments and low estrogen levels, worsened by her genetic tendency for hair loss.

The document concludes that new treatments for hair loss may involve a combination of cosmetics, clinical methods, and genetic approaches.

The meeting highlighted major advances in skin research, including new findings on skin microbes, genetic links to skin diseases, and improved treatments for various conditions.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

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.

Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Cancer development is like natural selection, involving mutated cells and environmental factors.

Alopecia areata involves complex immune and genetic factors, with potential treatment targets identified, but more research is needed.

The 2024 guideline updates recommendations for genetic testing, imaging, and sperm retrieval in male infertility.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

About 15% of adolescent girls in a region of India have Polycystic Ovarian Syndrome, which is more common in those born by cesarean, with wisdom teeth, or with central obesity.

Stem cell niches are crucial for regulating stem cell behavior and tissue health, and their decline can impact aging and cancer.

Alopecia areata, a common autoimmune hair loss condition, often runs in families.

AGA more common in men, Koreans have lower rates and unique patterns.

Alopecia areata is a genetic and immune-related hair loss condition that is often associated with other autoimmune diseases and does not typically cause permanent damage to hair follicles.

The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Hair loss in black women needs more research, early intervention, and community education.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

Hair can indicate early signs of metabolic disorders, with issues like protein deficiency stopping hair growth.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Antiviral medication valganciclovir may improve skin and hair in Trichodysplasia Spinulosa patients.

A 10-year-old boy had the earliest reported case of hair that became progressively kinkier but eventually returned to normal on its own.

Mutation in hairless gene may increase hair loss risk.

Frontal Fibrosing Alopecia is a poorly understood condition that is hard to treat and causes distressing hair loss.