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People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Sensory neuron and Merkel-cell changes in the skin happen independently during normal skin maintenance.

Stress during pregnancy can thin fetal skin.

A 14-year-old girl with no menstrual period was diagnosed with Swyer Syndrome and treated for a related cancer risk.

CD98hc's role in skin health decreases with age.

A rare benign skin growth called melanocytic matricoma was identified in a 69-year-old man.

Overexpression of the glucocorticoid receptor in mice causes developmental defects similar to ectodermal dysplasia.

The method effectively creates acellular dermal matrix from pig skin while preserving structure.

Fibromodulin treatment helps reduce scarring and improves wound healing by making it more like fetal healing.

Males and females differ in lifespan, growth, organ size, metabolism, and brain structure, with females generally living longer and maturing earlier.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

Neonatal blood vessels rearrange and stabilize as adults, with adult vessels better at self-repair after injury.

The document says menstruation is important for women's health, discusses menstrual disorders, and suggests personalized treatment options.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

MED1 affects skin wound healing differently in young and old mice.

The Foxn1 gene is essential for normal nail and hair development.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

Genetic hair shaft abnormalities can be seen with microscopes and often affect scalp hair.

Lack of a key enzyme causes severe skin issues and death in mice.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Hydrogel surface properties affect mouse embryoid body differentiation.

Conditions affecting sex development show that sexual diversity is a natural part of human variation.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Human skin has less GDNF and its receptor with age.

Sensory neuron remodeling and Merkel-cell changes in the skin happen independently.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Melasma skin has more melanin and signs of aging, with strong CK10 expression linked to cell differentiation and aging.

Rural Bangladeshi girls mature later than peers in other low and middle-income countries due to poor nutrition and socioeconomic conditions.

EAAT4 decreases with age, harming skin function and calcium balance.