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

Eclipta alba (Bhringaraja) has many medicinal uses, including protecting the liver, promoting hair growth, and reducing inflammation.

Patients with Frontal fibrosing alopecia in Morocco often have skin conditions and thyroid disorders.

ECCL should be considered in patients with specific skin and eye lesions.

Choosing the right model order in brain connectivity analysis can affect the detection of differences between healthy individuals and those with seasonal affective disorder.

Selenium-enriched green tea might be a safe prebiotic for gut health.

The red Hibiscus rosa-sinensis flower has the highest antioxidant activity.

UV light might cause excessive hair growth by increasing PGE2 in the skin.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

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

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Melatonin protects skin against UV damage by regulating various cellular processes.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

HPV vaccines are generally safe but need further investigation for rare side effects.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

Researchers concluded that "spigo nardo" is the Himalayan plant Nardostachys jatamansi, used historically in medicine and cosmetics, now critically endangered.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

The document explains the genetic causes and characteristics of inherited hair disorders.

Lower GPX4 mRNA levels are linked to higher disease activity and symptoms in lupus patients.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

Male pattern hair loss may have evolved to promote younger fathers for offspring health and survival, encouraging monogamy and paternal nurturing.

KCNQ potassium channels help control the sensitivity of touch receptors in the skin.

Dystonia may be part of PAS-4 and linked to immune issues.

The twins' condition is unique and doesn't match any known syndromes.

Finasteride, a drug, can block the seizure-preventing effects of a hormone called progesterone in mice.

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

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Valproic acid can cause a skin condition called leukocytoclastic vasculitis, which usually gets better after stopping the drug.