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A specific gene mutation causes varying hair loss severity in a Pakistani family.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Finger length ratio may indicate male hair loss.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Mutations in specific genes cause different types of ectodermal dysplasias.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Vitiligo and alopecia areata may share common causes.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

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

Pigmentary mosaicism causes skin color changes and can affect multiple body systems, but has no cure.

Polarized microscopy helps identify hair irregularities in genetic disorders.

A specific gene mutation causes a severe skin disorder in a family.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

A 24-year-old man developed both alopecia areata universalis and type 1 diabetes at the same time, which is rare.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

A unique hair tumor with a rippled pattern was identified, showing incomplete differentiation and unusual cell arrangements.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.