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Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

Adrenal disorders can cause lasting brain and behavior issues in children.

Stress, nutritional issues, and chronic diseases can cause hair loss, and nail changes may signal internal diseases; treatment focuses on the underlying cause.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

A 23-year-old man has a benign, non-progressive hair loss patch that doesn't respond to treatment but can be cosmetically treated.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Dermoscopy helps accurately diagnose temporal triangular alopecia, avoiding unnecessary treatments.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

Testosterone and its metabolites affect brain functions and could help treat neurological disorders.

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.

Trichotillomania is more common than previously thought, with increasing diagnosed cases.

Light microscopy is useful for diagnosing different hair disorders.

Hair color is influenced by genetics and can indicate certain health conditions.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

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

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

People with Down's syndrome often have more skin problems due to a weak immune system.

Children with alopecia areata should only get thyroid screening if they have Down syndrome, a family history of thyroid disease, atopy, or signs of thyroid problems.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.