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Diabetic patients often have ingrown nails due to obesity, high blood pressure, past injuries, bad nail trimming, nail fungus, weak foot pulse, and weak knee reflex.

The four patients have a unique type of ichthyosis affecting hair follicles.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Darier-White disease causes skin and nail issues, starts around age 20, worsens until 40-50, and has poor treatment options.

A child with rough nails also had hair loss and allergies.

The patient showed signs of liver disease due to alcohol use but didn't need treatment for Dupuytren’s contracture.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

New genetic mutations linked to rare skin disorders were found in three newborns.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

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

Woolly hair syndrome is a genetic condition causing frizzy, fragile hair.

DPR can cause skin, hair, and nail issues, sometimes appearing later in life.

Two Australian Poll Hereford calves had severe anaemia, abnormal red blood cells, and skin issues.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Two new gene mutations cause a rare hair disorder.

Epidermolysis bullosa is a genetic disease causing fragile skin and blisters in both animals and humans.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

A 3-year-old girl has short anagen syndrome, causing her hair to stay short.

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Excessive body hair can signal complex health issues.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

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

Netherton's syndrome may have a familial link and doesn't always include atopy.

Digit ratio likely doesn't predict male hair loss.