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Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

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

Poor quality hair products contribute to premature greying in children.

Genetic and lifestyle factors influence skin and hair aging, and prediction models can help assess aging and cosmetic treatments.

Elderly people often have skin issues like wrinkles, dryness, and benign tumors, needing special dermatology care.

Thymoma may link myasthenia gravis, nail dystrophy, and alopecia areata.

A boy with GAPO syndrome had hair loss similar to male pattern baldness without hormone issues, possibly due to skin or blood vessel problems.

MAEG helps in mouse hair follicle development by aiding cell adhesion.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Glycyrrhizin may help regrow hair by activating a specific pathway.

A parasite-derived molecule speeds up skin healing and affects immune cell behavior without increasing scarring.

Severe malnutrition in young children causes various skin and nail issues, mainly pigmentation changes and extreme thinness.

Polarized microscopy helps identify hair irregularities in genetic disorders.

Tight hairstyles can cause a rare scalp condition with thick skin folds.

A specific gene mutation causes sparse, brittle hair in a family.

The girl has a hormonal imbalance causing increased hair growth and other male characteristics.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

Teens with PCOS have a higher risk of type 2 diabetes and need regular glucose checks.

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

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Premature greying in kids can signal health issues like vitamin deficiencies or thyroid problems, which can be treated.

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

BOOST is a promising, easy-to-use treatment for diabetic foot ulcers that improves healing by reducing inflammation and promoting blood vessel growth.

Premature hair graying in young Turkish adults is more likely if they have stress, a family history of graying, drink alcohol, have chronic diseases, are older, or are taller.

Gp₄G promotes hair growth and improves skin health.

Hydrocortisone ointment effectively improved eyebrow skin and hair in a 10-year-old.