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Thyroid disease can cause hair loss and treating thyroid problems might help with hair disorders.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Hormones significantly affect hair and oil gland function in the skin, and more research is needed on skin-related hormone disorders.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

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.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Certain genes are linked to the risk of developing Alopecia Areata.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

Alopecia areata is a common autoimmune disease affecting about 2% of people, causing significant disability and often associated with mental health issues and other autoimmune conditions.

Obesity is linked to various skin problems and may increase the risk of skin cancer.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Androgenetic alopecia involves genetics, hormones, and can be treated with medications or surgery.

Hormones, especially androgens, play a key role in acne, which can be a symptom of systemic diseases like PCOS and may require targeted treatment.

Acne is a chronic disease linked to various systemic conditions and has significant psychological and social effects.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

Men are more likely to get infectious skin diseases, while women are more prone to autoimmune and pigment-related skin conditions, influenced by biological and environmental factors.

Marie Antoinette syndrome causes sudden hair whitening, but its exact cause is unknown.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

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

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.