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A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

A new change in the WNT10A gene caused a condition leading to short hair growth in a Chinese family.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

FGF5 gene mutations cause long hair in domestic cats.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Female and male AGA are different diseases.

Genetic counselors should be culturally skilled and aware of transgender patients' unique health risks and needs.

Pygmy goats with seborrhoeic dermatitis showed skin symptoms and temporary improvement with corticosteroids, but the cause and inheritance of the disease remain unknown.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

A mother and daughter with similar hair loss conditions and identical HLA types suggest a genetic link between the conditions.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Longer hair loss leads to more severe CCCA; early treatment and avoiding damaging hairstyles help regrowth.

A woman showed neurological symptoms from psittacosis linked to bird exposure, improving after antibiotic treatment.

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Finasteride caused blisters on hands and feet.

Chesapeake Bay retrievers' hair loss is likely a breed-specific, hereditary condition linked to abnormal steroid levels and distinct skin changes.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Understanding how androgens work is key for creating new treatments for prostate issues and hair/skin conditions.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.