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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

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

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

A specific gene mutation causes severe skin and nail issues and hair loss.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

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

Sun exposure and genetics increase skin cancer risk from precancerous lesions.

A new gene mutation linked to a skin condition was found in a Spanish family.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Genetic research may lead to better ways to predict and treat male-pattern hair loss.

A new gene mutation is linked to monilethrix in the studied family.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Alopecia areata, a common autoimmune hair loss condition, often runs in families.

Uncombable hair is inherited dominantly with complete penetrance.

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

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

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

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

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

A specific gene mutation causes congenital hair loss.

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

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

New genetic variants linked to albinism were found in Pakistani families.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.