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A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Tortoiseshell tomcats with XX/XY chimerism can be fertile.

Some families have a genetic condition where they are born with irregular scalp defects.

Hair form in mixed-blood families varies due to hereditary twist-knots and pigment formation.

Gene expression, especially Dkk4, is key to cat color patterns.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

All major hair defects involve cuticle abnormalities.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

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

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

A gene mutation in mice causes permanent hair loss and skin issues.

Genetic defects in androgen production are linked to male developmental disorders and are improving treatment understanding.

A girl had rickets due to a gene mutation affecting vitamin D response.

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

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Male children's genital development issues can be caused by genetic mutations or environmental factors affecting hormone action.

Genetic mutations can affect female sexual development, requiring personalized medical care.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

C57BL/6 mice and SD rats have different sweat gland and hair follicle patterns, useful for skin research.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.

Hair loss in certain mice is linked to changes in keratin-related genes.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

A 54-year-old woman experienced progressive hair loss starting in adolescence, leading to sparse scalp hair and almost no eyebrows or eyelashes.

Two mouse mutations cause similar hair loss despite different skin changes.

Genetics may play a significant role in gender dysphoria.

Mutation in hairless gene may increase hair loss risk.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.