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The complement system might be involved in the development of alopecia areata and could lead to new treatments.

Long-haul COVID can cause lasting symptoms affecting many body systems and may be linked to ongoing inflammation and immune system issues.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Surgical robots have improved but still can't perform tasks or make decisions on their own.

Genetic discoveries are leading to new treatments for alopecia areata.

Plasma-activated liquid can kill harmful cells, speed up wound healing, and potentially treat cancer without damaging healthy cells.

Some vitamins and minerals are important for preventing hair loss, but treating hair loss with them without a known deficiency is not proven effective.

Isotretinoin therapy for acne can cause many reversible side effects, mainly mild skin conditions, and patient understanding of these effects can improve treatment adherence.

Origanum vulgare leaf extract reduces liver and kidney damage caused by finasteride in mice.

Losartan may help treat Postural Orthostatic Tachycardia Syndrome (POTS) symptoms.

Early baldness in men may indicate risks for obesity, metabolic syndrome, insulin resistance, and heart disease, similar to women with PCOS. Alopecia areata is often linked with autoimmune diseases and mental health issues. Certain hair disorders are due to genetic issues, and chemotherapy can cause hair loss through specific biological pathways. Iron deficiency's link to hair loss is still disputed.

Oral Minoxidil can cause serious eye problems, but stopping it can improve vision.

Non-biologic immunosuppressive drugs are crucial for treating autoimmune and chronic inflammatory skin diseases.

The pandemic likely caused delays in skin cancer assessments, leading to fewer early diagnoses and thicker melanomas.

The document concludes that correct diagnosis of alopecia types is crucial, scalp biopsies are important, and more research is needed.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Treating cystoid macular oedema in uveitis is difficult and risky.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

Men taking dutasteride may have a higher risk of age-related macular degeneration.

Hair loss might be linked to eye aging due to inflammation markers in blood.

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

Using a call center to collect data in a trial for eye disease in diabetics led to high response rates and very little missing information.

Finasteride and dutasteride may cause macular abnormalities.

Women with PCOS have thicker parafoveal areas in their retinas, but their macular blood vessel density is normal.

The document discusses challenges in eye care, including treating melanoma before macular hole repair, bloody tears resolved by blood pressure control, eyelash regrowth in hair-pulling disorder with medication, a non-invasive method to detect eyelash mites, and the psychological factors affecting contact lens comfort.