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CDH3-related disease causes worsening eye and hair issues.

Some skin lymphomas can look like common skin issues and need careful testing to diagnose correctly.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Macular alopecia is a distinct, non-scarring hair loss pattern that mostly affects young Hispanic/Latinx females and often resolves on its own.

Using a diode laser for hair removal without eye protection can cause serious eye injuries.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

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

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

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

A new genetic mutation was found causing hair and eye issues in a boy.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Men taking dutasteride may have a higher risk of age-related macular degeneration.

Hair loss might be linked to eye aging due to inflammation markers in blood.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

wAMD patients have higher oxidative stress, suggesting antioxidant treatment may help.

Skin changes help detect graft-versus-host reaction early after bone marrow transplants.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

The body can heal and achieve remarkable states through specific mind-body practices.

Finasteride and dutasteride may cause macular abnormalities.

Children with darker skin tones can have specific skin conditions that need tailored treatments.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Scientists can mimic hair disorders by altering genes in lab-grown human hair follicles, but these follicles lack some features of natural ones.