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A Western diet may increase acne risk, while a Mediterranean diet and certain supplements can help reduce it.

Stocking rate affects wool follicle inactivity, not Merino strain.

Longer anogenital distance may indicate a higher chance of having polycystic ovary syndrome, and measuring this distance along with hormone levels could improve diagnosis.

Prostate cancer prevention now focuses on healthy diets and some medications, not vitamins.

Olive and olive oil help prevent and manage heart diseases.

Diet and lifestyle changes can help manage autoimmune diseases by reducing inflammation and supporting immune health.

Rosemary has many health benefits and is used in medicine and cosmetics.

Reptiles on the Absheron Peninsula accumulate toxic elements in their tissues but survive due to tissue resilience.

The guidelines suggest lifestyle changes, diet adjustments, and personalized medication to manage dyslipidemia and reduce heart disease risk.

Excessive hair growth in women often has no known cause and is not linked to race or other hormonal symptoms.

An 18-year-old girl with pemphigus vulgaris needed strong medication and careful treatment due to ineffective initial therapies and side effects.

Vitamin D deficiency is common in adults with muscle and bone pain, especially women.

The document explains different hair and scalp conditions, including common hair loss after pregnancy or illness, drug-induced hair loss, hereditary excessive hair growth, patterned baldness, autoimmune hair loss, and permanent loss due to skin disease, with generally limited treatment options.

Abraham's family infertility may have a genetic explanation.

Oxidative stress damages hair follicles and worsens hair loss in androgenetic alopecia.

Hirsutism is relatively common among young Greek women.

New JAK inhibitor drugs show promise for treating skin diseases but need more research on safety and effectiveness.

Laser hair removal is safe for people with Systemic Lupus Erythematosus.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A mutant FERONIA gene affects root hair growth at high temperatures.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Some people have a genetic variation that makes them less effective at breaking down drugs.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.