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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.

Darier-White disease causes skin and nail issues, starts around age 20, worsens until 40-50, and has poor treatment options.

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.

Prolactin levels and gene polymorphism are not linked to vitiligo severity but are related to BMI.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

Higher levels of miR-203 may contribute to hair loss in alopecia areata.

People with Down's syndrome are more likely to have syringomas.