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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Hair loss in men is mainly caused by hormones and genes, and while current treatments can slow it down, they can't fully stop it.

New drug shows promise for better hair growth in baldness treatment.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

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

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

AGA, a common hair loss, is caused by genetics, hormones, age, and environmental factors.

A three-year-old girl has hair loss despite treatment with selenium sulfide shampoo and anti-fungal medication.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

More research is needed to understand sex and racial differences in long COVID.

A new gene mutation causes insulin resistance in a girl and her mother.

A new gene variant causes glucocorticoid resistance in a mother and son.

People with Down syndrome have higher rates of certain immune-related conditions and need special medical attention.

The safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

The essay suggests hair loss might be caused by changes in skull bones.

A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

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

High TSPEAR levels in colorectal cancer predict worse outcomes.

High TSPEAR levels in colorectal cancer predict worse outcomes.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

Two sisters have rare hair disorders causing short, fragile, kinky hair.