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A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

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

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

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

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

The document concludes that more multidisciplinary research is needed to understand and treat PCOS, a condition that significantly affects women's health and quality of life.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Researchers found a genetic region that influences the number of coat layers in dogs.

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

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The study found nine new hair protein genes in human hair follicles.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

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

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Monilethrix has no effective treatment, but avoiding hair trauma helps manage it.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

Two specific genetic markers increase the risk of hair loss in Asian populations.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

A girl inherited excessive body hair from her mother and grandmother.