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Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Some skin conditions may indicate metabolic syndrome, which could help with early detection and management of related health issues.

The document explains how to identify different hair problems using a microscope.

COVID-19 can cause various skin problems, including reactions to protective gear and medication, with different rates reported worldwide, and more research is needed to fully understand these skin issues.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

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.

The index to ring finger ratio may indicate disease severity in female ankylosing spondylitis patients, but not in males.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Orchid callus extract can help hair grow and may be used in eco-friendly hair products.

Blood type affects COVID-19 infection rates differently in Europe and Africa.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Trichoscopy is crucial for diagnosing and assessing alopecia areata in children.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

A single long white eyelash is a rare but benign condition.

Cosmetic products or emotional factors might contribute to Frontal Fibrosing Alopecia, and trichoscopy is useful for diagnosis.

Phenoxyethanol in hair growth products may be linked to frontal fibrosing alopecia.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

A vitamin D receptor mutation causes rickets and affects immune responses.

Genomic research can help improve the quality and production of natural fibers in animals.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Gastric bypass surgery improved a woman's hormonal disorder without the need for medication.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Skin emergency severity rises with other health issues and affects multiple organs; a new grading system can improve patient care.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.