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The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The meeting showcased rare skin disease cases, highlighting the need for accurate diagnosis and treatment.

A man developed neurological issues from SARS-CoV-2 without severe breathing problems, worsening to death.

Biotinidase deficiency has various symptoms and can be treated with biotin supplements.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Biotin treatment improves symptoms of biotinidase deficiency, but some neurological damage may be permanent.

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

The girl had a rare disorder causing mental and physical symptoms, with weak hair and unclear neurological issues.

The document concludes that early diagnosis of Balint's syndrome is crucial for effective treatment and that understanding drug interactions, like between ritonavir and statins, is important for patient care.

A rare biotin deficiency in an Iraqi family caused severe symptoms but was successfully treated with lifelong biotin.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Some steroid-induced health issues in rodents improved after stopping treatment, but hair loss and eye problems did not.

Genetic testing for EGFR mutations is crucial in similar cases.

Diphenyl cresyl phosphate has low toxicity but can harm the liver, kidneys, adrenal glands, and testicles at high doses.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

Golden oyster mushroom extract may protect skin cells from aging by its antioxidant properties.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

Finasteride blocks deoxycorticosterone's anticonvulsant effects in infant rats, but indomethacin doesn't.

17α-estradiol is a safe estrogen that might protect the brain and doesn't cause feminization, needing more research for treating brain diseases.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

A woman's liver problems improved after she stopped taking spironolactone.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

Treating epilepsy is complex, requiring careful drug choice and patient adherence to manage seizures and side effects.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

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

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.