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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.

Botanical extracts can help treat hair loss in people with certain genetic conditions.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

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

Neurotrophins, especially NGF, are crucial for pain development and management.

Mouse genital development depends on male or female hormones for specific features.

Higher early lead exposure is linked to delayed puberty in girls.

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

Microglia, the brain's immune cells, may contribute to Polycystic Ovary Syndrome (PCOS) by altering the female brain's structure and function, with kisspeptin neurons and GABA neurotransmitters also playing a role.

A baby girl had two brain-related growths removed and is developing normally.

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

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

High levels of androgens during early development may cause PCOS-like symptoms.

Recent progress has been made in understanding inherited hair and nail disorders.

Female guinea pigs exposed to less allopregnanolone before birth showed more anxiety-like behavior.

Low birthweight and rapid weight gain after birth may increase the risk of developing polycystic ovary syndrome.

Doctors are preparing to potentially perform uterus transplants in transgender women, considering technical, hormonal, and ethical factors.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Thallium is highly toxic, causing severe health issues, and Prussian blue is the best antidote.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Inclusive and affirming healthcare is essential for improving transgender individuals' quality of life and health.

The manuscript "Strīvilāsa" offers ancient Ayurvedic knowledge on women's health, beauty treatments, and reproductive care.

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.

Experts discussed treatments for skin conditions in children, emphasizing hydration, cautious medication use, and early intervention for infections.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

Certain finger length ratios and body hair patterns may predict side effects from birth control pills in women.

The conclusion is that hair supplement ingredients may be unsafe and should be disclosed and proven safe before use.

Early skin biopsy helps diagnose and manage severe skin conditions in babies.

The document concludes that the exact way alcohol causes harm to fetal development is unknown, but it significantly affects nutrient transport to the fetus and a safe level of alcohol during pregnancy is not determined.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.