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A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Higher androgen levels during puberty are linked to shorter adult height in boys with Silver-Russell syndrome.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

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.

Gene mutations can cause problems in male genital development.

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.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

ATP-sensitive K+ channel subunits, particularly Sur2A, play a significant role in various cancers.

Robotic hair transplantation with AI offers more reliable, precise, and efficient hair restoration.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

A mother's diet at conception can cause lasting genetic changes in her child.

Maternal stress during pregnancy affects a child's stress levels.

A mother's PPARγ is crucial for preventing harmful milk that can cause inflammation and growth problems in babies.

Mothers and newborns with dental fillings had higher mercury in their hair, but getting fillings during pregnancy didn't raise mercury levels further.

A mother's western diet can make her milk toxic, causing inflammation and hair loss in babies.

Eating glucoraphanin can help prevent psychosis in offspring whose mothers had immune system activation.

High levels of male hormones in pregnant mice cause heart enlargement and poor heart function in their female babies.

Maternal Nano-Se supplements improve fetal hair follicle development in cashmere goats.

Newborns' hair shows how much caffeine their mothers drank during pregnancy.

Monkeys with hair loss during pregnancy showed higher stress hormone levels and invested differently in their offspring.

Too much male hormone in mothers can negatively affect the sexual behavior of both male and female baby mice.

A mother's iron levels early in pregnancy can influence the DNA makeup of her child, potentially affecting the child's health.

Mothers and newborns with dental fillings have higher mercury in their hair, but adding fillings during pregnancy doesn't raise mercury levels further.

Fetal-maternal stem cells in a mother's hair can help with tissue repair and regeneration long after childbirth.

Proper diagnosis is crucial to avoid overtreatment and complications in pregnant women with hyperthyroidism.

The commentary stresses the importance of using historical control data and proper interpretation in evaluating developmental toxicity.