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Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Ichthyoses are genetic skin disorders that affect the skin's barrier function.

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

Hirosaki hairless rats have sparse, twisted hair due to missing hair keratin genes.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Iron deficiency in mothers causes hair loss in their baby mice.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

Biotinidase deficiency can mimic neuromyelitis optica and should be considered for accurate diagnosis and treatment.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

Researchers found a non-functional sheep keratin gene due to mutations.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

A 6-year-old girl's inability to grow her hair long was due to Loose Anagen Hair Syndrome, which causes hair to shed easily and may improve with age.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

The research identified unique metabolic activities in immune cells associated with hair loss in Alopecia Areata.

A woman with a specific mutation causing adrenal gland issues faced fertility problems, but careful hormone therapy helped her manage it successfully.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

A new gene mutation causes a rare type of hair loss.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.