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A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

A genetic variant in the KRT25 gene causes tightly curled hair.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Live vaccines can be safely given to infants with a FOXN1 variant if their immune function improves over time.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

The CORIN gene variant causes the golden color in Siberian cats.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

5% topical minoxidil improves hair density and quality in monilethrix patients.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

A mutation in the KRT25 gene causes woolly hair and hair loss.

Certain genetic variants in keratins increase the risk of tooth decay.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Lykoi cats' unique sparse hair is linked to specific genetic variants in the Hairless gene.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

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

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.