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The document concludes that androgenetic alopecia is common, has a genetic link, and can be diagnosed and treated with medications like finasteride and minoxidil.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

Topical 5-Fluorouracil can rarely cause nerve damage, especially in people with a certain genetic deficiency.

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.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

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.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

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

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

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.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Transplanted hair follicles can resist hair loss from an autoimmune condition better than natural hair.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

New genetic locations explain much of hair color variation in Europeans.

Abnormal scalp whorls can indicate brain development issues but may also be seen in neurologically normal people.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

Frontal fibrosing alopecia and androgenetic alopecia may be related, with a possible shared cause.

Obesity changes androgen levels in women with PCOS, leading to higher testosterone relative to androstenedione.

Alopecia areata causes hair loss due to an immune attack on hair follicles, influenced by genetics and environment.

Androgens contribute to common male hair loss; more research needed for hair growth medication.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

Six genetic conditions are often linked to complete scalp hair loss in children.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

Genetic research may lead to better ways to predict and treat male-pattern hair loss.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.