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Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

The guideline recommends mental health involvement in diagnosing gender identity disorder and outlines hormone and surgical treatment protocols, emphasizing safety, informed consent, and long-term monitoring.

AGA causes hair loss by shrinking hair follicles due to DHT binding, and can be treated with finasteride and minoxidil.

Estrogens significantly influence hair growth by interacting with receptors in hair follicles and may help regulate the hair growth cycle.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Children with atopic dermatitis often have sleep problems, affecting their growth and behavior.

Children with atopic dermatitis often have sleep problems due to itching and may benefit from melatonin, which helps with sleep and skin symptoms.

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

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

Short anagen syndrome involves a hair growth phase lasting 1.5 years.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Certain zinc transporters are essential for healthy skin and managing zinc in the body could help treat skin problems.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

The document explains the genetic causes and characteristics of inherited hair disorders.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Chemotherapy causes hair loss by damaging hair follicles and stem cells, with more research needed for prevention and treatment.

Use minoxidil for hair loss; finasteride and dutasteride for men, dutasteride for women.

Treatment with plasma rich in growth factors improved hair density and thickness for hair loss patients.

DNA methylation changes are linked to hair growth cycles in goats.